A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571887



Internal ID20944958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:128981209..128982043hg38UCSC Ensembl
chr5:128316902..128317736hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg38835
hg19835
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267285
Samples
Known GenesSLC27A6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571887
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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