A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251272



Internal ID20818312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67413529..67413809hg38UCSC Ensembl
chr1:67879212..67879492hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545497
Supporting Variants
Samples
Known GenesSERBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251272
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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