A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491277



Internal ID21148830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23501474..23504767hg38UCSC Ensembl
chr14:23970683..23973976hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg383294
hg193294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016737
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491277
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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