A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768531



Internal ID19307794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67719305..67758737hg38UCSC Ensembl
chr9:46387499..46423100hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3839433
hg1935602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077127
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768531
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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