A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563104



Internal ID20936175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20052171..24804275hg38UCSC Ensembl
chr6:20052402..24804503hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384752105
hg194752102
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270143
Samples
Known GenesACOT13, ALDH5A1, C6orf62, CASC14, CASC15, CDKAL1, DCDC2, E2F3, GMNN, GPLD1, HDGFL1, KAAG1, KIAA0319, LINC00581, LOC101928603, MBOAT1, MRS2, NRSN1, PRL, SOX4, TDP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563104
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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