A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043437



Internal ID19132656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:76548540..76622681hg38UCSC Ensembl
Innerchr13:77122675..77196816hg19UCSC Ensembl
Innerchr13:76020676..76094817hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3874142
hg1974142
hg1874142
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530510
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)nsv1043437
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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