A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492109



Internal ID21149662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62654801..62655183hg38UCSC Ensembl
chr14:63121519..63121901hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020096
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492109
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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