A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540851



Internal ID20914139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62445758..62446838hg38UCSC Ensembl
chr1:62911429..62912509hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250542
Samples
Known GenesUSP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540851
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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