A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449467



Internal ID21107020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104116749..104119619hg38UCSC Ensembl
chr10:105876507..105879377hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg382871
hg192871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977736
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449467
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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