A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357626



Internal ID21015179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126295309..126331333hg38UCSC Ensembl
chr3:126014152..126050176hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3836025
hg1936025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094051
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357626
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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