A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448559



Internal ID21106112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104344567..104348112hg38UCSC Ensembl
chr10:106104325..106107870hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg383546
hg193546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977744
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448559
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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