A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16998200



Internal ID66345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66920779..66921066hg38UCSC Ensembl
chr7:66385766..66386053hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485688
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16998200
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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