A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568488



Internal ID20941559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151851546..151853130hg38UCSC Ensembl
chr6:152172681..152174265hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381585
hg191585
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269405
Samples
Known GenesESR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568488
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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