A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441460



Internal ID21099013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31765430..31767219hg38UCSC Ensembl
chr10:32054358..32056147hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg381790
hg191790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441460
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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