A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446577



Internal ID21104130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22981363..22982142hg38UCSC Ensembl
chr10:23270292..23271071hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38780
hg19780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979703
Samples
Known GenesARMC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446577
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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