A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441126



Internal ID21098679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14658662..14660876hg38UCSC Ensembl
chr10:14700661..14702875hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382215
hg192215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978732
Samples
Known GenesFAM107B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441126
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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