A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379421



Internal ID21036974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88204462..88210633hg38UCSC Ensembl
chr4:89125614..89131785hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg386172
hg196172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121815
Samples
Known GenesABCG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379421
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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