A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899617



Internal ID22674748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126524098..126529359hg38UCSC Ensembl
chr3:126242941..126248202hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg385262
hg195262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398725
Samples
Known GenesCHST13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899617
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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