A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274937



Internal ID20841977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67253536..72561415hg38UCSC Ensembl
chr7:66718523..72026400hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg385307880
hg195307878
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571906
Supporting Variants
Samples
Known GenesAUTS2, CALN1, LOC100507468, LOC101929736, MIR3914-1, MIR3914-2, PMS2P4, STAG3L4, TYW1B, WBSCR17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274937
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00178


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