A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491236



Internal ID21148789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24494701..24529200hg38UCSC Ensembl
chr14:24963907..24998406hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3834500
hg1934500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016220
Samples
Known GenesCMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491236
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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