A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448151



Internal ID21105704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13097601..13103900hg38UCSC Ensembl
chr10:13139601..13145900hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980687
Samples
Known GenesCCDC3, OPTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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