A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343110



Internal ID21000663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:104591737..104633565hg38UCSC Ensembl
chr2:105208195..105250023hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3841829
hg1941829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18076601
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343110
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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