A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105972



Internal ID21269048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:156835637..156840812hg38UCSC Ensembl
Innerchr3:156553426..156558601hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg385176
hg195176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113990
Supporting Variants
Samplessample134
Known GenesLEKR1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105972
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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