A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511537



Internal ID20884865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93136563..93145729hg38UCSC Ensembl
chr14:93602908..93612074hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg389167
hg199167
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511537
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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