A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17535682



Internal ID21860037
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 StatusS
Merged Variantsnsv5982840
Supporting Variants
Samples
Known GenesZNF678
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17535682
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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