A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558457



Internal ID20931528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87270113..87270574hg38UCSC Ensembl
chr5:86565930..86566391hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269696
Samples
Known GenesRASA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558457
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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