A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697592



Internal ID15087558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:36734507..36745943hg38UCSC Ensembl
Innerchr6:36702284..36713720hg19UCSC Ensembl
Innerchr6:36810262..36821698hg18UCSC Ensembl
Innerchr6:36810262..36821698hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3811437
hg1911437
hg1811437
hg1711437
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520755
Supporting Variants
Samples
Known GenesCPNE5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697592
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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