A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115162



Internal ID19271746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:72382547..72382952hg38UCSC Ensembl
Outerchr13:72956685..72957090hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv997n106
Supporting Variantsnssv3976213
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115162
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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