A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767448



Internal ID19314183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17127474..17127536hg38UCSC Ensembl
chr8:16984983..16985045hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075538
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767448
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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