A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585262



Internal ID20958333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75495101..75496894hg38UCSC Ensembl
chr11:75206146..75207939hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg381794
hg191794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234318
Samples
Known GenesGDPD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585262
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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