A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039213



Internal ID19128432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:42645975..42669655hg38UCSC Ensembl
Innerchr13:43220111..43243791hg19UCSC Ensembl
Innerchr13:42118111..42141791hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3823681
hg1923681
hg1823681
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523401
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)nsv1039213
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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