A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132856



Internal ID19248137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:36794644..36794723hg38UCSC Ensembl
Outerchr13:37368781..37368860hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv950n106
Supporting Variantsnssv3987649
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132856
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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