A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515267



Internal ID20888626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97635890..97648376hg38UCSC Ensembl
chr14:98102227..98114713hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3812487
hg1912487
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180155
Samples
Known GenesLOC100129345
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515267
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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