A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561099



Internal ID20934170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35676182..35775356hg38UCSC Ensembl
chr7:35715792..35814966hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3899175
hg1999175
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275597
Samples
Known GenesHERPUD2, LOC100506725
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561099
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