A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093311



Internal ID20660351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108459725..108460355hg38UCSC Ensembl
chr3:108178572..108179202hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367624
Supporting Variants
Samples
Known GenesMYH15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093311
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00067


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