A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580427



Internal ID20953498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30407869..30408338hg38UCSC Ensembl
chr11:30429416..30429885hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235707
Samples
Known GenesMPPED2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580427
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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