A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968268



Internal ID22743204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28831490..29349953hg38UCSC Ensembl
chr6:28799267..29317730hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38518464
hg19518464
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431500
Samples
Known GenesC6orf100, HCG14, LOC100129636, LOC401242, OR14J1, OR2B3, OR2J2, OR2J3, OR2W1, TRIM27, ZNF311
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968268
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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