A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495244



Internal ID21152797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35889410..35897961hg38UCSC Ensembl
chr14:36358616..36367167hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg388552
hg198552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017314
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495244
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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