A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352566



Internal ID21010119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:163251222..163251829hg38UCSC Ensembl
chr2:164107732..164108339hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079260
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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