A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102459



Internal ID22011694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39509857..39778283hg38UCSC Ensembl
chr1:39975529..40243955hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38268427
hg19268427
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526208
Samples
Known GenesBMP8A, BMP8B, HEYL, HPCAL4, NT5C1A, OXCT2, PABPC4, PPIE, PPIEL, SNORA55
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102459
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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