A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437982



Internal ID21095535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50714939..50731538hg38UCSC Ensembl
chr10:52474699..52491298hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3816600
hg1916600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190514
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437982
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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