A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16998802



Internal ID66780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77257675..77266485hg38UCSC Ensembl
chr7:76886992..76895802hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg388811
hg198811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490391
Supporting Variants
Samples
Known GenesCCDC146
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16998802
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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