A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582823



Internal ID18881104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:145095234..145161489hg38UCSC Ensembl
Innerchr2:145852801..145919056hg19UCSC Ensembl
Innerchr2:145569271..145635526hg18UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3866256
hg1966256
hg1866256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004846
Supporting Variants
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)nssv3582823
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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