A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478525



Internal ID21136078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81364633..81365176hg38UCSC Ensembl
chr14:81830977..81831520hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021397
Samples
Known GenesSTON2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478525
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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