A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14084600



Internal ID21274468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155295960..155299929hg38UCSC Ensembl
Innerchr7:155087670..155091639hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg383970
hg193970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110999
Supporting Variants
Samplessample208
Known GenesINSIG1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14084600
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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