A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3992424



Internal ID19226218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:90056945..90057267hg38UCSC Ensembl
Outerchr8:91069173..91069495hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140917
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3992424
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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