A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904201



Internal ID3620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63680255..63680388hg38UCSC Ensembl
chr1:64145926..64146059hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425484
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904201
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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