A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438269



Internal ID21095822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96528709..96529106hg38UCSC Ensembl
chr10:98288466..98288863hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985936
Samples
Known GenesTM9SF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438269
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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