A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346478



Internal ID21004031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135246867..135311730hg38UCSC Ensembl
chr2:136004437..136069300hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg3864864
hg1964864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077879
Samples
Known GenesZRANB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346478
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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