A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442503



Internal ID21100056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77366397..77377638hg38UCSC Ensembl
chr10:79126155..79137396hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3811242
hg1911242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984330
Samples
Known GenesKCNMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442503
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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