A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371655



Internal ID21029208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21824067..21830045hg38UCSC Ensembl
chr3:21865559..21871537hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385979
hg195979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099235
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371655
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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