A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590181



Internal ID20963252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71290200..71290993hg38UCSC Ensembl
chr14:71756917..71757710hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2192n223
Supporting Variantsnssv18238596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590181
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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