A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477913



Internal ID21135466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32199728..32202693hg38UCSC Ensembl
chr14:32668934..32671899hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg382966
hg192966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017817
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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