A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554113



Internal ID20927222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:30938278..30938858hg38UCSC Ensembl
chr1:31411125..31411705hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252379
Samples
Known GenesPUM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554113
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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