A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587658



Internal ID20960729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39000965..39001354hg38UCSC Ensembl
chr14:39470169..39470558hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227073
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587658
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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