A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389967



Internal ID21047520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42441201..42443300hg38UCSC Ensembl
chr4:42443218..42445317hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116413
Samples
Known GenesATP8A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389967
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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