A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553177



Internal ID20926286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:48790806..48807653hg38UCSC Ensembl
chr1:49256478..49273325hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3816848
hg1916848
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251177
Samples
Known GenesAGBL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553177
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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