A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998726



Internal ID19191503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:70102461..70106090hg38UCSC Ensembl
Outerchr8:71014696..71018325hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg383630
hg193630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1149940
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998726
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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