A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553704



Internal ID20926815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27844876..27845210hg38UCSC Ensembl
chr1:28171387..28171721hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249055
Samples
Known GenesPPP1R8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553704
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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