A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545372



Internal ID20918603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28698793..28699587hg38UCSC Ensembl
chr1:29025305..29026099hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38795
hg19795
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252320
Samples
Known GenesGMEB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545372
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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