A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521132



Internal ID15101739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9768841..9771659hg38UCSC Ensembl
Innerchr17:9672158..9674976hg19UCSC Ensembl
Innerchr17:9612883..9615701hg18UCSC Ensembl
Innerchr17:9612883..9615701hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg382819
hg192819
hg182819
hg172819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv176n21
Supporting Variantsnssv682803, nssv682676
Samples
Known GenesDHRS7C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521132
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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