A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352814



Internal ID21010367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:226159314..226164242hg38UCSC Ensembl
chr2:227024030..227028958hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg384929
hg194929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084192
Samples
Known GenesLOC646736
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352814
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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