A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571139



Internal ID20944210
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 Variantsdgv6883n223
Supporting Variantsnssv18274318
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)nsv6571139
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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