A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964448



Internal ID18886629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:152348808..152349135hg38UCSC Ensembl
Outerchr2:153205322..153205649hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121218
Supporting Variants
SamplesKWS2
Known GenesFMNL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964448
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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