A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676079



Internal ID15412731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6203166..6227773hg38UCSC Ensembl
Innerchr17:6106486..6131093hg19UCSC Ensembl
Innerchr17:6047210..6071817hg18UCSC Ensembl
Innerchr17:6047210..6071817hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3824608
hg1924608
hg1824608
hg1724608
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517031
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676079
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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