A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443510



Internal ID21101063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14015569..14019414hg38UCSC Ensembl
chr10:14057568..14061413hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383846
hg193846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978708
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443510
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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