A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345253



Internal ID21002806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:67569262..67570588hg38UCSC Ensembl
chr2:67796394..67797720hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg381327
hg191327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345253
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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