A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763951



Internal ID18958832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18793940..18794916hg38UCSC Ensembl
chr8:18651450..18652426hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38977
hg19977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074752
Supporting Variants
SamplesKWP1
Known GenesPSD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763951
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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