A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574155



Internal ID20947226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108182269..108182977hg38UCSC Ensembl
chr6:108503473..108504181hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38709
hg19709
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269837
Samples
Known GenesNR2E1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574155
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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