A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265162



Internal ID20832202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39553595..39554617hg38UCSC Ensembl
chr4:39555215..39556237hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381023
hg191023
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574852
Supporting Variants
Samples
Known GenesMIR1273H, SMIM14, UGDH-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265162
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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