A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578243



Internal ID20951314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118863114..118863761hg38UCSC Ensembl
chr11:118733823..118734470hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38648
hg19648
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1322n223
Supporting Variantsnssv18234615
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578243
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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