A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238725



Internal ID20805765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22854169..22854691hg38UCSC Ensembl
chr15:23018377..23018899hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576870
Supporting Variants
Samples
Known GenesNIPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238725
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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