A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108608



Internal ID21293091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:202738070..202741229hg38UCSC Ensembl
Innerchr1:202707198..202710357hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg383160
hg193160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118049
Supporting Variants
Samplessample96
Known GenesKDM5B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108608
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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