A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539965



Internal ID20913260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19635094..19637197hg38UCSC Ensembl
chr1:19961588..19963691hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg382104
hg192104
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248176
Samples
Known GenesMINOS1-NBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539965
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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