A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372653



Internal ID21030206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127675691..127680930hg38UCSC Ensembl
chr3:127394534..127399773hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg385240
hg195240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094110
Samples
Known GenesABTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372653
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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