A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036852



Internal ID20603892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51361965..51368723hg38UCSC Ensembl
chr17:49439326..49446084hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg386759
hg196759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516133
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036852
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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