A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275431



Internal ID20842471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5998081..5998652hg38UCSC Ensembl
chr7:6037712..6038283hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574592
Supporting Variants
Samples
Known GenesPMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275431
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00026


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