A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3571304



Internal ID18869585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:3847117..3875579hg38UCSC Ensembl
Innerchr2:3894707..3923169hg19UCSC Ensembl
Innerchr2:3872582..3901044hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3828463
hg1928463
hg1828463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003752
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)nssv3571304
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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