A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038269



Internal ID19127488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:82840309..82867419hg38UCSC Ensembl
Innerchr13:83414444..83441554hg19UCSC Ensembl
Innerchr13:82312445..82339555hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3827111
hg1927111
hg1827111
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530543
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)nsv1038269
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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