A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559794



Internal ID20932865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67035832..72791575hg38UCSC Ensembl
chr7:66500819..72256588hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg385755744
hg195755770
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6883n223
Supporting Variantsnssv18274323
Samples
Known GenesAUTS2, CALN1, LOC100507468, LOC101929736, MIR3914-1, MIR3914-2, MIR4650-1, MIR4650-2, PMS2P4, STAG3L4, TYW1, TYW1B, WBSCR17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559794
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