A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417375



Internal ID196573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25767167..25767379hg38UCSC Ensembl
chr1:26093658..26093870hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900382
Samples
Known GenesMAN1C1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417375
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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