A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590618



Internal ID20963689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21349090..21350279hg38UCSC Ensembl
chr14:21817249..21818438hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381190
hg191190
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2053n223
Supporting Variantsnssv18224981
Samples
Known GenesRPGRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590618
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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