A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519902



Internal ID15100509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:74840873..74854994hg38UCSC Ensembl
Innerchr17:72837012..72851133hg19UCSC Ensembl
Innerchr17:70348607..70362728hg18UCSC Ensembl
Innerchr17:70348607..70362728hg17UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3814122
hg1914122
hg1814122
hg1714122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv659423, nssv680704
Samples
Known GenesGRIN2C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519902
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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