A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548359



Internal ID20921546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19611603..19612375hg38UCSC Ensembl
chr1:19938097..19938869hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38773
hg19773
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv110n223
Supporting Variantsnssv18248172
Samples
Known GenesMINOS1, MINOS1-NBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548359
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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