A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352105



Internal ID21009658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6091851..6126413hg38UCSC Ensembl
chr2:6231983..6266545hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3834563
hg1934563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352105
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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