A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448902



Internal ID21106455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76046358..76051131hg38UCSC Ensembl
chr10:77806116..77810889hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg384774
hg194774
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187229
Samples
Known GenesC10orf11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448902
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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