A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672239



Internal ID15062205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1708905..1745000hg38UCSC Ensembl
Innerchr17:1612199..1648294hg19UCSC Ensembl
Innerchr17:1558949..1595044hg18UCSC Ensembl
Innerchr17:1558949..1595044hg17UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3836096
hg1936096
hg1836096
hg1736096
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516886
Supporting Variants
Samples
Known GenesMIR22, MIR22HG, SERPINF2, TLCD2, WDR81
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672239
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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