A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547830



Internal ID20921030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86944035..86944372hg38UCSC Ensembl
chr1:87409718..87410055hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251912
Samples
Known GenesHS2ST1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547830
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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