A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034017



Internal ID20601057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10330357..10395451hg38UCSC Ensembl
chr17:10233674..10298768hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3865095
hg1965095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499779
Supporting Variants
Samples
Known GenesMYH13, MYH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034017
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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