A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595128



Internal ID20968199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103596129..103597033hg38UCSC Ensembl
chr14:104062466..104063370hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38905
hg19905
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2251n223
Supporting Variantsnssv18231630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595128
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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