A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18002659



Internal ID20569699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:67755018..67755598hg38UCSC Ensembl
chr12:68148798..68149378hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473716
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18002659
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00047


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