A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3571323



Internal ID18869604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4158085..4175101hg38UCSC Ensembl
Innerchr2:4205675..4222691hg19UCSC Ensembl
Innerchr2:4183550..4200566hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3817017
hg1917017
hg1817017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013159
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)nssv3571323
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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