A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557741



Internal ID20930812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:103095932..103097894hg38UCSC Ensembl
chr5:102431636..102433598hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg381963
hg191963
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266467
Samples
Known GenesGIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557741
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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