A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557928



Internal ID20930999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:118006963..118008193hg38UCSC Ensembl
chr5:117342658..117343888hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg381231
hg191231
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5911n223
Supporting Variantsnssv18266647
Samples
Known GenesLOC102467224
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557928
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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