A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140218



Internal ID339411
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 StatusM
Merged Variants
Supporting Variantsnssv16898255
Samples
Known GenesZNF678
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140218
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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