A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251207



Internal ID20818247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50648311..50649137hg38UCSC Ensembl
chr1:51113983..51114809hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38827
hg19827
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540382
Supporting Variants
Samples
Known GenesFAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251207
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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