A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345338



Internal ID21002891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64611223..64616327hg38UCSC Ensembl
chr2:64838357..64843461hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg385105
hg195105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089315
Samples
Known GenesLOC339807
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345338
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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