A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14084629



Internal ID21275025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:68701312..68707084hg38UCSC Ensembl
Innerchr7:68166299..68172071hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg385773
hg195773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116725
Supporting Variants
Samplessample216
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14084629
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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