A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564604



Internal ID20937675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61457517..61458878hg38UCSC Ensembl
chr5:60753344..60754705hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg381362
hg191362
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5776n223
Supporting Variantsnssv18269131
Samples
Known GenesZSWIM6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564604
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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