A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037158



Internal ID20604198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62130403..62133069hg38UCSC Ensembl
chr17:60207764..60210430hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg382667
hg192667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522019
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037158
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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