A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613210



Internal ID16053933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6635045..6750556hg38UCSC Ensembl
Innerchr9:6635045..6750556hg19UCSC Ensembl
Innerchr9:6625045..6740556hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38115512
hg19115512
hg18115512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12488n54
Supporting Variantsnssv1126541, nssv1126540
Samples
Known GenesGLDC, KDM4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613210
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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