A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16995408



Internal ID64371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39662322..39662383hg38UCSC Ensembl
chr7:39701921..39701982hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484449
Supporting Variants
Samples
Known GenesRALA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16995408
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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