A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527570



Internal ID15454863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:64972926..64980940hg38UCSC Ensembl
Innerchr2:65200060..65208074hg19UCSC Ensembl
Innerchr2:65053564..65061578hg18UCSC Ensembl
Innerchr2:65111711..65119725hg17UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg388015
hg198015
hg188015
hg178015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704031
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527570
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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