A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349698



Internal ID21007251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:222937201..222938300hg38UCSC Ensembl
chr2:223801919..223803018hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086956
Samples
Known GenesACSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349698
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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