A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567679



Internal ID20940750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125860350..125862052hg38UCSC Ensembl
chr6:126181496..126183198hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg381703
hg191703
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271174
Samples
Known GenesNCOA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567679
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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