A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596481



Internal ID20969552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18146557..18147628hg38UCSC Ensembl
chr20:18127201..18128272hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg381072
hg191072
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4422n223
Supporting Variantsnssv18253616
Samples
Known GenesCSRP2BP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596481
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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