A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229252



Internal ID20796292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158832286..159197356hg38UCSC Ensembl
chr7:158624977..158990045hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38365071
hg19365069
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420716
Supporting Variants
Samples
Known GenesLINC00689, VIPR2, WDR60
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229252
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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