A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352225



Internal ID21009778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:106164948..106165421hg38UCSC Ensembl
chr2:106781404..106781877hg19UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18076667
Samples
Known GenesUXS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352225
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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