A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041552



Internal ID19130771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55575752..55684045hg38UCSC Ensembl
Innerchr13:56149887..56258179hg19UCSC Ensembl
Innerchr13:55047888..55156180hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38108294
hg19108293
hg18108293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1658n100
Supporting Variantsnssv3523867
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)nsv1041552
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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