A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669170



Internal ID21617475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:63729712..63844058hg38UCSC Ensembl
chr7:63190090..63304436hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38114347
hg19114347
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148031
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669170
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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