A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655807



Internal ID15392459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:28321466..28373451hg38UCSC Ensembl
Innerchr17:26648492..26700470hg19UCSC Ensembl
Innerchr17:23672619..23724597hg18UCSC Ensembl
Innerchr17:23672619..23724597hg17UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3851986
hg1951979
hg1851979
hg1751979
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519388
Supporting Variants
Samples
Known GenesIFT20, MIR4723, POLDIP2, SARM1, SEBOX, TMEM199, TMEM97, TNFAIP1, VTN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655807
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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