A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438683



Internal ID21096236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122732676..122850848hg38UCSC Ensembl
chr10:124492192..124610364hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38118173
hg19118173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978232
Samples
Known GenesCUZD1, FAM24B, FAM24B-CUZD1, FLJ46361
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438683
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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