A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517242



Internal ID15444535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149759270..149839125hg38UCSC Ensembl
Innerchr7:149456359..149536214hg19UCSC Ensembl
Innerchr7:149087292..149167147hg18UCSC Ensembl
Innerchr7:148894007..148973862hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3879856
hg1979856
hg1879856
hg1779856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv683093, nssv654765, nssv664620, nssv679912, nssv654110, nssv661526, nssv663453, nssv689006, nssv655050, nssv662782, nssv666660, nssv692721, nssv662303, nssv682006, nssv685132, nssv683294, nssv677707
Samples
Known GenesSSPO, ZNF467, ZNF862
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517242
Frequency
Sample Size2026
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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