A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976262



Internal ID18264783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96266345..96272512hg38UCSC Ensembl
Innerchr13:96918599..96924766hg19UCSC Ensembl
Innerchr13:95716600..95722767hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg386168
hg196168
hg186168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2765811
SamplesHGDP01284
Known GenesHS6ST3
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976262
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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