A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762260



Internal ID19313696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65693845..65727646hg38UCSC Ensembl
chr9:70438399..70472200hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3833802
hg1933802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077151
Supporting Variants
SamplesKWP1
Known GenesCBWD3, CBWD5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762260
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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