A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583019



Internal ID18881300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:168414178..168441444hg38UCSC Ensembl
Innerchr2:169270688..169297954hg19UCSC Ensembl
Innerchr2:168978934..169006200hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3827267
hg1927267
hg1827267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002508
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)nssv3583019
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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