A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044671



Internal ID19133890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86409582..86447586hg38UCSC Ensembl
Innerchr13:87061837..87099841hg19UCSC Ensembl
Innerchr13:85859838..85897842hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3838005
hg1938005
hg1838005
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1720n100
Supporting Variantsnssv3525426
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)nsv1044671
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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