A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3975389



Internal ID19245672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:35270877..35270927hg38UCSC Ensembl
Outerchr8:35128395..35128445hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115086
Supporting Variants
SamplesKWS2
Known GenesUNC5D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3975389
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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