A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494540



Internal ID21152093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24598138..24607000hg38UCSC Ensembl
chr14:25067344..25076206hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg388863
hg198863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016228
Samples
Known GenesGZMH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494540
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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