A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16895920



Internal ID171445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221324538..221331922hg38UCSC Ensembl
chr1:221497880..221505264hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg387385
hg197385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444854
Supporting Variants
Samples
Known GenesC1orf140
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16895920
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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