A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999313



Internal ID19158849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:33899102..33984674hg38UCSC Ensembl
Innerchr4:33900724..33986296hg19UCSC Ensembl
Innerchr4:33577119..33662691hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3885573
hg1985573
hg1885573
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737775
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)nsv999313
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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