A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575532



Internal ID20948603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73557810..73558695hg38UCSC Ensembl
chr5:72853635..72854520hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38886
hg19886
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267076
Samples
Known GenesANKRA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575532
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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