A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967465



Internal ID18892674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:25457684..25458584hg38UCSC Ensembl
Outerchr8:25315200..25316100hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112960
Supporting Variants
SamplesKWS2
Known GenesKCTD9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967465
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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