A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274327



Internal ID20841367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67120589..72691764hg38UCSC Ensembl
chr7:66585576..72156754hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg385571176
hg195571179
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574039
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)nssv18274327
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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