A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546073



Internal ID20919293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26116352..26116899hg38UCSC Ensembl
chr1:26442843..26443390hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38548
hg19548
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251577
Samples
Known GenesPDIK1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546073
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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