A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440536



Internal ID21098089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9904947..10046295hg38UCSC Ensembl
chr10:9946910..10088258hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38141349
hg19141349
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183274
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440536
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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