A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498154



Internal ID20871362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96956454..96963459hg38UCSC Ensembl
chr14:97422791..97429796hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg387006
hg197006
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022478
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498154
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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