A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036930



Internal ID20603970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55549039..55553839hg38UCSC Ensembl
chr17:53626400..53631200hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg384801
hg194801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533990
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036930
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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