A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422842



Internal ID201877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25633103..25635674hg38UCSC Ensembl
chr1:25959594..25962165hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382572
hg192572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900242
Samples
Known GenesMAN1C1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422842
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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