A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042755



Internal ID19131974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:64726309..64825911hg38UCSC Ensembl
Innerchr13:65300441..65400043hg19UCSC Ensembl
Innerchr13:64198442..64298044hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3899603
hg1999603
hg1899603
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3526803
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)nsv1042755
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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