A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454089



Internal ID21111642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12137056..12139181hg38UCSC Ensembl
chr10:12179055..12181180hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382126
hg192126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980548
Samples
Known GenesSEC61A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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