A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986404



Internal ID18873529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:18597104..18598434hg38UCSC Ensembl
Outerchr8:18454614..18455944hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381331
hg191331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131834
Supporting Variants
SamplesKWS1
Known GenesPSD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986404
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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