A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003524



Internal ID19092742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:207469588..207495060hg38UCSC Ensembl
Innerchr2:208334312..208359784hg19UCSC Ensembl
Innerchr2:208042557..208068029hg18UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3825473
hg1925473
hg1825473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3585572
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003524
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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