A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694904



Internal ID15084870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:22177812..22258633hg38UCSC Ensembl
Innerchr17:21704418..21785239hg19UCSC Ensembl
Innerchr17:21628545..21709366hg18UCSC Ensembl
Innerchr17:21628545..21709366hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3880822
hg1980822
hg1880822
hg1780822
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516664
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694904
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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