A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037043



Internal ID20604083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57033089..57044773hg38UCSC Ensembl
chr17:55110450..55122134hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3811685
hg1911685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533370
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037043
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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