A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076168



Internal ID18979216
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 StatusM
Merged Variants
Supporting Variantsnssv3765787
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076168
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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