A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548304



Internal ID20921496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86969937..86970683hg38UCSC Ensembl
chr1:87435620..87436366hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251914
Samples
Known GenesHS2ST1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548304
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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