A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507900



Internal ID20881196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93327301..93332500hg38UCSC Ensembl
chr14:93793647..93798846hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183347
Samples
Known GenesBTBD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507900
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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