A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16949663



Internal ID33781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42585704..42585835hg38UCSC Ensembl
chr4:42587721..42587852hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470624
Supporting Variants
Samples
Known GenesATP8A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16949663
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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