A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536110



Internal ID20909464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10184607..10188283hg38UCSC Ensembl
chr1:10244665..10248341hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg383677
hg193677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536110
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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