A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251397



Internal ID20818437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:72686736..72688323hg38UCSC Ensembl
chr1:73152419..73154006hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg381588
hg191588
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552714
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251397
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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