A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453381



Internal ID21110934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36565251..36576592hg38UCSC Ensembl
chr10:36854179..36865520hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3811342
hg1911342
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182704
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453381
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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