A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966564



Internal ID19234863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:107368486..107368866hg38UCSC Ensembl
Outerchr8:108380714..108381094hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112474
Supporting Variants
SamplesKWS2
Known GenesANGPT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966564
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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