A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14082811



Internal ID21290412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:1098007..1104391hg38UCSC Ensembl
Innerchr6:1098242..1104626hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg386385
hg196385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111698
Supporting Variants
Samplessample6
Known GenesLOC285768
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14082811
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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