A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445999



Internal ID21103552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123055267..123056229hg38UCSC Ensembl
chr10:124814783..124815745hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38963
hg19963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978440
Samples
Known GenesACADSB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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