A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579882



Internal ID20952953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52580606..52581076hg38UCSC Ensembl
chr14:53047324..53047794hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218053
Samples
Known GenesGPR137C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579882
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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