A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451812



Internal ID21109365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14939980..15021932hg38UCSC Ensembl
chr10:14981979..15063931hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3881953
hg1981953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv615n223
Supporting Variantsnssv17978746
Samples
Known GenesDCLRE1C, MEIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451812
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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