A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584092



Internal ID20957163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71290040..71290779hg38UCSC Ensembl
chr14:71756757..71757496hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38740
hg19740
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2192n223
Supporting Variantsnssv18238595
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584092
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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