A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520755



Internal ID15101362
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv379n21
Supporting Variantsnssv697592
Samples
Known GenesCPNE5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520755
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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