A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248094



Internal ID20815134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171578002..171578686hg38UCSC Ensembl
chr1:171547141..171547825hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38685
hg19685
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546833
Supporting Variants
Samples
Known GenesPRRC2C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248094
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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