A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486406



Internal ID21143959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21538051..22772225hg38UCSC Ensembl
chr14:22006185..23241434hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381234175
hg191235250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016026
Samples
Known GenesABHD4, DAD1, OR10G2, OR10G3, OR4E2, OXA1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486406
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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