A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558580



Internal ID20931651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15097989..15099726hg38UCSC Ensembl
chr6:15098220..15099957hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381738
hg191738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558580
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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