A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348925



Internal ID21006478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64816010..64817822hg38UCSC Ensembl
chr2:65043144..65044956hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg381813
hg191813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089321
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348925
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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