A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454098



Internal ID21111651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95448943..95490985hg38UCSC Ensembl
chr10:97208700..97250742hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3842043
hg1942043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985736
Samples
Known GenesSORBS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454098
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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