A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712997



Internal ID136663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38925934..38925985hg38UCSC Ensembl
chr17:37082187..37082238hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517791
Supporting Variants
Samples
Known GenesLINC00672
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712997
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001405


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