A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481942



Internal ID21139495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45350801..45547000hg38UCSC Ensembl
chr14:45820004..46016203hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38196200
hg19196200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2131n223
Supporting Variantsnssv18018756
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481942
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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