A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450203



Internal ID21107756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29294739..29562997hg38UCSC Ensembl
chr10:29583668..29851926hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38268259
hg19268259
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181150
Samples
Known GenesLYZL1, MIR604, PTCHD3P1, SVIL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450203
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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