A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540858



Internal ID20914146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50594247..50595140hg38UCSC Ensembl
chr1:51059919..51060812hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38894
hg19894
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251199
Samples
Known GenesFAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540858
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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