A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962672



Internal ID19216951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:168863099..168863156hg38UCSC Ensembl
Outerchr3:168580887..168580944hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129240
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962672
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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