A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342016



Internal ID20999569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65592118..65661299hg38UCSC Ensembl
chr2:65819252..65888433hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3869182
hg1969182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342016
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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