A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251152



Internal ID20818192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:4728817..4913703hg38UCSC Ensembl
chr1:4788877..4973763hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38184887
hg19184887
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537510
Supporting Variants
Samples
Known GenesAJAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251152
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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