A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112999



Internal ID19262617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67653171..67656560hg38UCSC Ensembl
Outerchr9:46311700..46315100hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg383390
hg193401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967883
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112999
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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