A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544217



Internal ID20917456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87009947..87011086hg38UCSC Ensembl
chr1:87475630..87476769hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg381140
hg191140
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv256n223
Supporting Variantsnssv18251915
Samples
Known GenesHS2ST1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544217
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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