A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352961



Internal ID21010514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69114035..69117275hg38UCSC Ensembl
chr2:69341167..69344407hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg383241
hg193241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088874
Samples
Known GenesANTXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352961
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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