A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569464



Internal ID20942535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146136513..146138188hg38UCSC Ensembl
chr5:145516076..145517751hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381676
hg191676
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268012
Samples
Known GenesLARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569464
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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