A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006906



Internal ID21916249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13683123..13683816hg38UCSC Ensembl
chr10:13725123..13725816hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590034
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006906
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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