A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562731



Internal ID20935802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13646688..13648028hg38UCSC Ensembl
chr4:13648312..13649652hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg381341
hg191341
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5190n223
Supporting Variantsnssv18263127
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562731
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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