A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996866



Internal ID20563906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10077846..10078198hg38UCSC Ensembl
chr12:10230445..10230797hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464289
Supporting Variants
Samples
Known GenesCLEC1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996866
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00148


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