A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964146



Internal ID19233401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:85231793..85232608hg38UCSC Ensembl
Outerchr8:86144022..86144837hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120936
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964146
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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