A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453813



Internal ID21111366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13083101..13091800hg38UCSC Ensembl
chr10:13125101..13133800hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980672
Samples
Known GenesCCDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453813
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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