A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673652



Internal ID15410304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:28303453..28379927hg38UCSC Ensembl
Innerchr17:26630479..26706946hg19UCSC Ensembl
Innerchr17:23654606..23731073hg18UCSC Ensembl
Innerchr17:23654606..23731073hg17UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3876475
hg1976468
hg1876468
hg1776468
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519388
Supporting Variants
Samples
Known GenesIFT20, KRT18P55, MIR4723, POLDIP2, SARM1, SEBOX, TMEM199, TMEM97, TNFAIP1, VTN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673652
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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