A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037546



Internal ID20604586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68552650..68552980hg38UCSC Ensembl
chr17:66548791..66549121hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517587
Supporting Variants
Samples
Known GenesFAM20A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037546
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.20359


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