A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051640



Internal ID19140859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:54569291..54904412hg38UCSC Ensembl
Innerchr13:55143426..55478547hg19UCSC Ensembl
Innerchr13:54041427..54376548hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38335122
hg19335122
hg18335122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1656n100
Supporting Variantsnssv3714985
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)nsv1051640
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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