A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965025



Internal ID18899937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:94773955..94774237hg38UCSC Ensembl
Outerchr10:47088415..47088697hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129889
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965025
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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