A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037976



Internal ID20605016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71159604..71169407hg38UCSC Ensembl
chr17:69155745..69165548hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg389804
hg199804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518291
Supporting Variants
Samples
Known GenesCASC17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037976
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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