A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247823



Internal ID20814863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179143756..179144311hg38UCSC Ensembl
chr1:179112891..179113446hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554494
Supporting Variants
Samples
Known GenesABL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247823
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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