A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699804



Internal ID15089770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:63928647..63979250hg38UCSC Ensembl
Innerchr17:62006007..62056610hg19UCSC Ensembl
Innerchr17:59359739..59410342hg18UCSC Ensembl
Innerchr17:59359739..59410342hg17UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3850604
hg1950604
hg1850604
hg1750604
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517272
Supporting Variants
Samples
Known GenesCD79B, SCN4A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699804
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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