A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745550



Internal ID20521560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77376556..77376639hg38UCSC Ensembl
chr10:79136314..79136397hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276812
Samples
Known GenesKCNMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745550
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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