A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14084244



Internal ID21269340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156948808..156952127hg38UCSC Ensembl
Innerchr7:156741502..156744821hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg383320
hg193320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113999
Supporting Variants
Samplessample138
Known GenesNOM1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14084244
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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