A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556000



Internal ID20929071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149669303..149669955hg38UCSC Ensembl
chr6:149990439..149991091hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38653
hg19653
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6449n223
Supporting Variantsnssv18269285
Samples
Known GenesLATS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556000
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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