A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968743



Internal ID18257285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:106977369..106979277hg38UCSC Ensembl
Innerchr9:109739650..109741558hg19UCSC Ensembl
Innerchr9:108779471..108781379hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381909
hg191909
hg181909
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2564627, nssv2564620, nssv2564622, nssv2564628, nssv2564626, nssv2564623, nssv2564624, nssv2564621, nssv2564629, nssv2564625
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesMIR548Q, ZNF462
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968743
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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