A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553780



Internal ID20926893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19600776..19601378hg38UCSC Ensembl
chr1:19927270..19927872hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38603
hg19603
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248171
Samples
Known GenesMINOS1, MINOS1-NBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553780
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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