A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345858



Internal ID21003411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135324747..135328804hg38UCSC Ensembl
chr2:136082317..136086374hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg384058
hg194058
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204878
Samples
Known GenesZRANB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345858
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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