A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957677



Internal ID18874530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:133066688..133066738hg38UCSC Ensembl
Outerchr5:132402380..132402430hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128190
Supporting Variants
SamplesKWS1
Known GenesHSPA4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957677
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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