A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480800



Internal ID21138353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30962012..30964751hg38UCSC Ensembl
chr14:31431218..31433957hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg382740
hg192740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017742
Samples
Known GenesSTRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480800
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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