A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489531



Internal ID21147084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:42014333..42017538hg38UCSC Ensembl
chr14:42483536..42486741hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg383206
hg193206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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