A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765787



Internal ID18958352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39047996..39085935hg38UCSC Ensembl
chr9:65645699..65687900hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3837940
hg1942202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076168
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765787
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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