A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553490



Internal ID20926599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28747832..28749413hg38UCSC Ensembl
chr1:29074344..29075925hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381582
hg191582
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252326
Samples
Known GenesYTHDF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553490
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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