A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147196



Internal ID346378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164537844..164548601hg38UCSC Ensembl
chr5:163964850..163975607hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3810758
hg1910758
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976530
Samples
Known GenesLOC102546299
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147196
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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