A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440805



Internal ID21098358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77551630..77615723hg38UCSC Ensembl
chr10:79311388..79375481hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3864094
hg1964094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984337
Samples
Known GenesKCNMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440805
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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