A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437397



Internal ID21094950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124844996..124858156hg38UCSC Ensembl
chr10:126533565..126546725hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3813161
hg1913161
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437397
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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