A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764237



Internal ID19313545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67854053..67855154hg38UCSC Ensembl
chr9:67921499..67922600hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077142
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764237
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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