A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543360



Internal ID20916609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77852926..77853448hg38UCSC Ensembl
chr1:78318611..78319133hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253172
Samples
Known GenesFAM73A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543360
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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