A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671396



Internal ID15408048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6203166..6217722hg38UCSC Ensembl
Innerchr17:6106486..6121042hg19UCSC Ensembl
Innerchr17:6047210..6061766hg18UCSC Ensembl
Innerchr17:6047210..6061766hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3814557
hg1914557
hg1814557
hg1714557
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)nssv671396
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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