A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274410



Internal ID20841450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139184793..139350399hg38UCSC Ensembl
chr7:138869539..139035145hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38165607
hg19165607
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567612
Supporting Variants
Samples
Known GenesC7orf55, C7orf55-LUC7L2, LUC7L2, TTC26, UBN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274410
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