A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279937



Internal ID20489155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66565585..66793687hg38UCSC Ensembl
chr7:66030572..66258674hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38228103
hg19228103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735592
Supporting Variants
Samples
Known GenesKCTD7, LOC493754, RABGEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279937
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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