A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488970



Internal ID21146523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:46546201..46551600hg38UCSC Ensembl
chr14:47015404..47020803hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019094
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488970
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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