A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446793



Internal ID21104346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37866536..37869756hg38UCSC Ensembl
chr10:38155464..38158684hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg383221
hg193221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446793
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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