A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453847



Internal ID21111400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22864805..22869061hg38UCSC Ensembl
chr10:23153734..23157990hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg384257
hg194257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979698
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453847
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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