A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447495



Internal ID21105048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80523501..80526476hg38UCSC Ensembl
chr10:82283257..82286232hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg382976
hg192976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447495
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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