A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575628



Internal ID20948699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123673858..123674670hg38UCSC Ensembl
chr11:123544566..123545378hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1329n223
Supporting Variantsnssv18231503
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575628
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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