A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250983



Internal ID20818023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42670811..42671271hg38UCSC Ensembl
chr1:43136482..43136942hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536794
Supporting Variants
Samples
Known GenesPPIH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250983
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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