A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493633



Internal ID21151186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:48316901..48444800hg38UCSC Ensembl
chr14:48786104..48914003hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38127900
hg19127900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019509
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493633
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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