A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040959



Internal ID19130178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68429305..68625379hg38UCSC Ensembl
Innerchr13:69003437..69199511hg19UCSC Ensembl
Innerchr13:67901438..68097512hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38196075
hg19196075
hg18196075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1704n100
Supporting Variantsnssv3527949
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)nsv1040959
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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