A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492160



Internal ID21149713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:47699424..47699902hg38UCSC Ensembl
chr14:48168627..48169105hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019340
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492160
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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