A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978083



Internal ID20545123
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 StatusS
Merged Variantsnsv6443379
Supporting Variants
Samples
Known GenesCELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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