A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982840



Internal ID21892183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227654802..227655306hg38UCSC Ensembl
chr1:227842503..227843007hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38505
hg19505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535682
Samples
Known GenesZNF678
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982840
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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