A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962601



Internal ID19204742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:111631417..111631501hg38UCSC Ensembl
Outerchr13:112283764..112283848hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129171
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962601
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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