A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448353



Internal ID21105906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32346201..32349600hg38UCSC Ensembl
chr10:32635129..32638528hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178809
Samples
Known GenesEPC1, LOC102031319
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448353
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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