A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447322



Internal ID21104875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45068624..45072590hg38UCSC Ensembl
chr10:45564072..45568038hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383967
hg193967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980391
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447322
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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