A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16906978



Internal ID5437
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 StatusS
Merged Variantsnsv5424402
Supporting Variants
Samples
Known GenesALG14
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16906978
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.024828


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