A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667605



Internal ID21615910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5989047..6735643hg38UCSC Ensembl
chr7:6028678..6775274hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38746597
hg19746597
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152806
SamplesHG00731
Known GenesAIMP2, ANKRD61, C7orf26, CYTH3, DAGLB, EIF2AK1, FAM220A, GRID2IP, KDELR2, PMS2, PMS2CL, RAC1, USP42, ZDHHC4, ZNF12, ZNF316, ZNF853
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667605
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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