A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981263



Internal ID18871883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:26557763..26558163hg38UCSC Ensembl
Outerchr13:27131900..27132300hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143586
Supporting Variants
SamplesKWS1
Known GenesWASF3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981263
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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