A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443606



Internal ID21101159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84211107..84221207hg38UCSC Ensembl
chr10:85970863..85980963hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3810101
hg1910101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186131
Samples
Known GenesCDHR1, LRIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443606
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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