A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044736



Internal ID19133955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:76154519..76492299hg38UCSC Ensembl
Innerchr13:76728655..77066435hg19UCSC Ensembl
Innerchr13:75626656..75964436hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38337781
hg19337781
hg18337781
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530509
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)nsv1044736
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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