A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680704



Internal ID15070670
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519902
Supporting Variants
Samples
Known GenesGRIN2C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680704
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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