A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557197



Internal ID20930268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146348002..146348610hg38UCSC Ensembl
chr5:145727565..145728173hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268038
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557197
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer