A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133712



Internal ID19261656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:60856228..60858428hg38UCSC Ensembl
Outerchr9:41442500..41444700hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg382201
hg192201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969285
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133712
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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