A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484351



Internal ID21141904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75395784..75396461hg38UCSC Ensembl
chr14:75862487..75863164hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021130
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484351
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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