A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380485



Internal ID21038038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42656201..42658200hg38UCSC Ensembl
chr4:42658218..42660217hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213645
Samples
Known GenesATP8A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380485
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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