A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449189



Internal ID21106742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11096516..11103985hg38UCSC Ensembl
chr10:11138479..11145948hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg387470
hg197470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979523
Samples
Known GenesCELF2, CELF2-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449189
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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