A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762917



Internal ID19309238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38073781..38075282hg38UCSC Ensembl
chr8:37931299..37932800hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg381502
hg191502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075131
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762917
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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