A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447182



Internal ID21104735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116692617..116694244hg38UCSC Ensembl
chr10:118452128..118453755hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381628
hg191628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978274
Samples
Known GenesHSPA12A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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