A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548293



Internal ID20921485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109022729..109023043hg38UCSC Ensembl
chr1:109565351..109565665hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247286
Samples
Known GenesWDR47
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548293
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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