A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429840



Internal ID208675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12745324..12747071hg38UCSC Ensembl
chr1:12805272..12807019hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg381748
hg191748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16894370
Samples
Known GenesC1orf158
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429840
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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