A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671914



Internal ID21620221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39511549..39776456hg38UCSC Ensembl
chr1:39977221..40242128hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38264908
hg19264908
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065314
Samples
Known GenesBMP8A, BMP8B, HEYL, HPCAL4, NT5C1A, OXCT2, PABPC4, PPIE, PPIEL, SNORA55
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671914
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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