A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6883n223



Internal ID22809851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66977695..72844217hg38UCSC Ensembl
chr7:66442682..72314795hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg385866523
hg195872114
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6567352, nsv6571139, nsv6558198, nsv6565886, nsv6559794, nsv6557013, nsv6571906, nsv6571183, nsv6557201, nsv6574039, nsv6575171, nsv6574963
Samples
Known GenesAUTS2, CALN1, LOC100507468, LOC101929736, MIR3914-1, MIR3914-2, MIR4650-1, MIR4650-2, PMS2P4, SBDS, SBDSP1, STAG3L4, TYW1, TYW1B, WBSCR17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6883n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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