A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16997132



Internal ID65629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64316515..64316582hg38UCSC Ensembl
chr7:63776893..63776960hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479977
Supporting Variants
Samples
Known GenesZNF736
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16997132
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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