A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990139



Internal ID19245890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:42365373..42433271hg38UCSC Ensembl
Outerchr9:41007400..41075600hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3867899
hg1968201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137638
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990139
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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