A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424402



Internal ID203395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95004803..95005427hg38UCSC Ensembl
chr1:95470359..95470983hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38625
hg19625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16906978
Samples
Known GenesALG14
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424402
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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