A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036962



Internal ID20604002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55985417..55997336hg38UCSC Ensembl
chr17:54062778..54074697hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3811920
hg1911920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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