A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274427



Internal ID20841467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139670331..139671019hg38UCSC Ensembl
chr7:139355077..139355765hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38689
hg19689
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567437
Supporting Variants
Samples
Known GenesHIPK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274427
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