A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528400



Internal ID15455693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:235146445..235167112hg38UCSC Ensembl
Innerchr2:236055089..236075756hg19UCSC Ensembl
Innerchr2:235719828..235740495hg18UCSC Ensembl
Innerchr2:235837089..235857756hg17UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3820668
hg1920668
hg1820668
hg1720668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704990
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528400
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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