A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351599



Internal ID21009152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21462626..21463270hg38UCSC Ensembl
chr2:21685498..21686142hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38645
hg19645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351599
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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