A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16898255



Internal ID172976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227654809..227655332hg38UCSC Ensembl
chr1:227842510..227843033hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140218
Supporting Variants
Samples
Known GenesZNF678
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16898255
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.014205


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