A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213645



Internal ID20780685
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 StatusS
Merged Variantsnsv6380485
Supporting Variants
Samples
Known GenesATP8A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213645
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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