A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253127



Internal ID20820167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75495039..75608155hg38UCSC Ensembl
chr1:75960724..76073840hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38113117
hg19113117
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540128
Supporting Variants
Samples
Known GenesSLC44A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253127
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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