A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570559



Internal ID21762602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:955549..986801hg38UCSC Ensembl
chr7:995185..1026437hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3831253
hg1931253
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015040
Supporting Variants
Samples
Known GenesCOX19, CYP2W1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570559
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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