A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249956



Internal ID20816996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204539553..204540143hg38UCSC Ensembl
chr1:204508681..204509271hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546331
Supporting Variants
Samples
Known GenesMDM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249956
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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