A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965659



Internal ID19240275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:62550833..62553891hg38UCSC Ensembl
Outerchr2:62777968..62781026hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg383059
hg193059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111985
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965659
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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