A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274934



Internal ID20841974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67210891..72603125hg38UCSC Ensembl
chr7:66675878..72068110hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg385392235
hg195392233
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575171
Supporting Variants
Samples
Known GenesAUTS2, CALN1, LOC100507468, LOC101929736, MIR3914-1, MIR3914-2, PMS2P4, STAG3L4, TYW1, TYW1B, WBSCR17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274934
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