A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341884



Internal ID20999437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21505116..21505881hg38UCSC Ensembl
chr2:21727988..21728753hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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