A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516640



Internal ID15443933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:50498265..50501037hg38UCSC Ensembl
Innerchr7:50565963..50568735hg19UCSC Ensembl
Innerchr7:50533457..50536229hg18UCSC Ensembl
Innerchr7:50340172..50342944hg17UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg382773
hg192773
hg182773
hg172773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669818, nssv696578, nssv663014
Samples
Known GenesDDC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516640
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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