A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904801



Internal ID4021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40698420..40698864hg38UCSC Ensembl
chr1:41164092..41164536hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419271
Supporting Variants
Samples
Known GenesNFYC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904801
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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