A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563034



Internal ID20936105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42825141..42826443hg38UCSC Ensembl
chr6:42792879..42794181hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381303
hg191303
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6174n223
Supporting Variantsnssv18271322
Samples
Known GenesGLTSCR1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563034
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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