A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539396



Internal ID20861450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36045456..36047025hg38UCSC Ensembl
chr1:36511057..36512626hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381570
hg191570
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251037
Samples
Known GenesAGO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539396
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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