A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516074



Internal ID15443367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126496558..126513773hg38UCSC Ensembl
Innerchr9:129258837..129276052hg19UCSC Ensembl
Innerchr9:128298658..128315873hg18UCSC Ensembl
Innerchr9:126338391..126355606hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3817216
hg1917216
hg1817216
hg1717216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693344, nssv662913, nssv691344, nssv652475, nssv691320, nssv663690, nssv687949, nssv683251, nssv674212, nssv685326, nssv665192, nssv690143, nssv673729, nssv669633, nssv660878, nssv690298, nssv683359, nssv690276, nssv651899, nssv689908, nssv665852, nssv663749, nssv673039, nssv660446, nssv670624, nssv682719, nssv679915, nssv670670, nssv684379, nssv660464, nssv670020, nssv675327, nssv674356, nssv664622, nssv671536, nssv677933, nssv677486, nssv692697, nssv689691, nssv688804, nssv679721, nssv661528, nssv693886, nssv658423, nssv654879, nssv692438, nssv674762, nssv684608, nssv652301, nssv671215, nssv692862, nssv680849, nssv651838, nssv675713, nssv659446, nssv688566, nssv691892, nssv688353, nssv687039, nssv669616, nssv693453, nssv685219, nssv682505, nssv679514, nssv654977, nssv667812, nssv653738, nssv692020, nssv672606, nssv668694, nssv673612, nssv684290, nssv672650, nssv682308, nssv681989, nssv688680, nssv669989, nssv683205, nssv660222, nssv658608, nssv655375, nssv685784, nssv677781, nssv686460, nssv656375, nssv664840, nssv678179, nssv668323, nssv693305, nssv674187, nssv661094, nssv693589, nssv666270, nssv662571, nssv656024, nssv657519, nssv652950, nssv657267, nssv680180, nssv657674, nssv672023, nssv689108
Samples
Known GenesMVB12B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516074
Frequency
Sample Size2026
Observed Gain0
Observed Loss102
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer