A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567277



Internal ID20940348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:103530305..103535327hg38UCSC Ensembl
chr5:102866006..102871028hg19UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg385023
hg195023
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266472
Samples
Known GenesLOC102467212
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567277
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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