A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17002986



Internal ID69610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101622503..101622576hg38UCSC Ensembl
chr7:101265783..101265856hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476135
Supporting Variants
Samples
Known GenesMYL10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17002986
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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