A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562742



Internal ID20935813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42825296..42826588hg38UCSC Ensembl
chr6:42793034..42794326hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381293
hg191293
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6174n223
Supporting Variantsnssv18271323
Samples
Known GenesGLTSCR1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562742
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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