A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087708



Internal ID21275178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:71600744..71603562hg38UCSC Ensembl
Innerchr6:72310447..72313265hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg382819
hg192819
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116240
Supporting Variants
Samplessample218
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087708
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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