A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250610



Internal ID20817650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64221151..64221814hg38UCSC Ensembl
chr1:64686834..64687497hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38664
hg19664
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538975
Supporting Variants
Samples
Known GenesUBE2U
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250610
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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