A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547666



Internal ID20920867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50735577..50736539hg38UCSC Ensembl
chr1:51201249..51202211hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38963
hg19963
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251623
Samples
Known GenesFAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547666
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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