A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442815



Internal ID21100368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125028367..125030789hg38UCSC Ensembl
chr10:126716936..126719358hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382423
hg192423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978042
Samples
Known GenesCTBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442815
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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