A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366568



Internal ID22592237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58292528..58328991hg38UCSC Ensembl
chr10:60052288..60088751hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3836464
hg1936464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922501
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366568
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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