A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252707



Internal ID20819747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92695963..92696357hg38UCSC Ensembl
chr1:93161520..93161914hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539067
Supporting Variants
Samples
Known GenesEVI5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252707
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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