A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996482



Internal ID18845068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:112502362..112502457hg38UCSC Ensembl
Outerchr9:115264642..115264737hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1147695
Supporting Variants
SamplesKWB1
Known GenesKIAA1958
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996482
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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