A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137609



Internal ID19270765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:11200791..11201591hg38UCSC Ensembl
Outerchr8:11058300..11059100hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990112
SamplesKWS2
Known GenesXKR6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137609
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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