A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580073



Internal ID18878354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:98243679..98261581hg38UCSC Ensembl
Innerchr2:98860142..98878044hg19UCSC Ensembl
Innerchr2:98226574..98244476hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3817903
hg1917903
hg1817903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005509
Supporting Variants
Samples
Known GenesVWA3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580073
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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