A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543445



Internal ID20916693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10111708..10112536hg38UCSC Ensembl
chr1:10171766..10172594hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38829
hg19829
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249204
Samples
Known GenesUBE4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543445
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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