A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004152



Internal ID70398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:110349934..110368035hg38UCSC Ensembl
chr7:109989991..110008092hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3818102
hg1918102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475629
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004152
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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