A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557454



Internal ID20930525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94362525..94362627hg38UCSC Ensembl
chr5:93698230..93698332hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267716
Samples
Known GenesKIAA0825
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557454
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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