A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16998820



Internal ID66790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77522008..77522074hg38UCSC Ensembl
chr7:77151325..77151391hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484809
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16998820
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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