A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440292



Internal ID21097845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49407340..49431964hg38UCSC Ensembl
chr10:50615386..50640010hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3824625
hg1924625
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178154
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440292
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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