A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480244



Internal ID21137797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73956131..74033594hg38UCSC Ensembl
chr14:74422834..74500297hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3877464
hg1977464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021433
Samples
Known GenesCCDC176, COQ6, ENTPD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480244
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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