A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453706



Internal ID21111259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36895341..36909846hg38UCSC Ensembl
chr10:37184269..37198774hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3814506
hg1914506
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180831
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453706
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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