A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486656



Internal ID21144209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87741462..87792183hg38UCSC Ensembl
chr14:88207806..88258527hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3850722
hg1950722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022441
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486656
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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