A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989992



Internal ID19241338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:126983057..126983657hg38UCSC Ensembl
Outerchr3:126701900..126702500hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136370
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989992
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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