A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342764



Internal ID21000317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:144885001..144885900hg38UCSC Ensembl
chr2:145642568..145643467hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078182
Samples
Known GenesTEX41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342764
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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