A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3974366



Internal ID19207557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:67815085..67815417hg38UCSC Ensembl
Outerchr8:68727320..68727652hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135709
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3974366
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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