A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571134



Internal ID20944205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:127415848..127416030hg38UCSC Ensembl
chr5:126751540..126751722hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267265
Samples
Known GenesMEGF10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571134
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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