A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372635



Internal ID21030188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:29145341..29148141hg38UCSC Ensembl
chr3:29186832..29189632hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg382801
hg192801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101412
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372635
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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