A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556516



Internal ID20929587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45839665..45854771hg38UCSC Ensembl
chr6:45807402..45822508hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3815107
hg1915107
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271984
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556516
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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