A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3994996



Internal ID19220201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:66183122..66207522hg38UCSC Ensembl
Outerchr9:43163700..43188100hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3824401
hg1924401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1144263
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3994996
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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