A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586904



Internal ID20959975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70932017..70932603hg38UCSC Ensembl
chr14:71398734..71399320hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2190n223
Supporting Variantsnssv18238584
Samples
Known GenesPCNX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586904
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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