A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687693



Internal ID15424345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:58630658..58631618hg38UCSC Ensembl
Innerchr17:56708019..56708979hg19UCSC Ensembl
Innerchr17:54063018..54063978hg18UCSC Ensembl
Innerchr17:54063018..54063978hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38961
hg19961
hg18961
hg17961
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515871
Supporting Variants
Samples
Known GenesTEX14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687693
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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