A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17002819



Internal ID69500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96342691..96356509hg38UCSC Ensembl
chr7:95972003..95985821hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3813819
hg1913819
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477739
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17002819
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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