A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926807



Internal ID22702034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77597805..77602428hg38UCSC Ensembl
chr10:79357563..79362186hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg384624
hg194624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357547
Samples
Known GenesKCNMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926807
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