A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557066



Internal ID20930137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139152554..139153281hg38UCSC Ensembl
chr4:140073708..140074435hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557066
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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