A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275622



Internal ID20842662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36519683..36520487hg38UCSC Ensembl
chr7:36559289..36560093hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38805
hg19805
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575214
Supporting Variants
Samples
Known GenesAOAH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275622
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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