A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578187



Internal ID20951258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71385900..71387114hg38UCSC Ensembl
chr14:71852617..71853831hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg381215
hg191215
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238599
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578187
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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