A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454504



Internal ID21112057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95692996..95694010hg38UCSC Ensembl
chr10:97452753..97453767hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381015
hg191015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985301
Samples
Known GenesTCTN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454504
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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