A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036143



Internal ID20603183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49882521..49884461hg38UCSC Ensembl
chr17:47959884..47961824hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg381941
hg191941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525518
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036143
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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