A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563367



Internal ID20936438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42503844..42518895hg38UCSC Ensembl
chr7:42543443..42558494hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3815052
hg1915052
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275947
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563367
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer