A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965677



Internal ID18895120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:165221625..165222143hg38UCSC Ensembl
Outerchr2:166078135..166078653hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112003
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965677
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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