A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439105



Internal ID21096658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120384088..120406318hg38UCSC Ensembl
chr10:122143600..122165830hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3822231
hg1922231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980480
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439105
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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