A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3995001



Internal ID19215003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67677963..67683961hg38UCSC Ensembl
Outerchr9:46343800..46349800hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385999
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1144266
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3995001
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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