A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558198



Internal ID20931269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67037488..72789965hg38UCSC Ensembl
chr7:66502475..72254980hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg385752478
hg195752506
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6883n223
Supporting Variantsnssv18274324
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)nsv6558198
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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