A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966901



Internal ID19246097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:71639170..71639504hg38UCSC Ensembl
Outerchr8:72551405..72551739hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130585
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966901
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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