A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767216



Internal ID19309805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17899520..17902885hg38UCSC Ensembl
chr9:17899518..17902883hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg383366
hg193366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077095
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767216
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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