A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911246



Internal ID22686459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45469344..45469582hg38UCSC Ensembl
chr10:45964792..45965030hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363192
Samples
Known GenesMARCH8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911246
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer