A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449174



Internal ID21106727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79262778..79263978hg38UCSC Ensembl
chr10:81022535..81023735hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983589
Samples
Known GenesZMIZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449174
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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