A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981996



Internal ID19219223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:142667382..142670582hg38UCSC Ensembl
Outerchr8:143748800..143752000hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg383201
hg193201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119190
Supporting Variants
SamplesKWS1
Known GenesJRK, PSCA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981996
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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