A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038626



Internal ID19127845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26888769..26907762hg38UCSC Ensembl
Innerchr13:27462906..27481899hg19UCSC Ensembl
Innerchr13:26360906..26379899hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3818994
hg1918994
hg1818994
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523214
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)nsv1038626
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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