A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526660



Internal ID15453953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:225318770..225324477hg38UCSC Ensembl
Innerchr2:226183487..226189194hg19UCSC Ensembl
Innerchr2:225891731..225897438hg18UCSC Ensembl
Innerchr2:226008992..226014699hg17UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg385708
hg195708
hg185708
hg175708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702988
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526660
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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