A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137408



Internal ID18916775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:139696694..139696758hg38UCSC Ensembl
Outerchr8:140708937..140709001hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976106
SamplesKWS2
Known GenesKCNK9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137408
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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