A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963199



Internal ID18886111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:152348866..152349142hg38UCSC Ensembl
Outerchr2:153205380..153205656hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120763
Supporting Variants
SamplesKWS2
Known GenesFMNL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963199
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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