A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477459



Internal ID21135012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:44931730..45030621hg38UCSC Ensembl
chr14:45400933..45499824hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3898892
hg1998892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018730
Samples
Known GenesFAM179B, KLHL28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477459
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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