A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250825



Internal ID20817865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32259403..32260101hg38UCSC Ensembl
chr1:32725004..32725702hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38699
hg19699
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539914
Supporting Variants
Samples
Known GenesLCK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250825
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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