A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475932



Internal ID21133485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32578735..32582498hg38UCSC Ensembl
chr14:33047941..33051704hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg383764
hg193764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017833
Samples
Known GenesAKAP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475932
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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