A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573751



Internal ID20946822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34111345..34120544hg38UCSC Ensembl
chr6:34079122..34088321hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg389200
hg199200
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271217
Samples
Known GenesGRM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573751
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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