A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452945



Internal ID21110498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110124507..110124982hg38UCSC Ensembl
chr10:111884265..111884740hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979486
Samples
Known GenesADD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452945
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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