A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572835



Internal ID20945906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173347548..173347793hg38UCSC Ensembl
chr4:174268699..174268944hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264470
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572835
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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