A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546835



Internal ID20920045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151657495..151658157hg38UCSC Ensembl
chr1:151629971..151630633hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249947
Samples
Known GenesSNX27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546835
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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