A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443379



Internal ID21100932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11178704..11181412hg38UCSC Ensembl
chr10:11220667..11223375hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382709
hg192709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978083
Samples
Known GenesCELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443379
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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