A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352752



Internal ID21010305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105604344..105607183hg38UCSC Ensembl
chr2:106220801..106223640hg19UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg382840
hg192840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18076641
Samples
Known GenesLOC285000
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352752
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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