A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853191



Internal ID22628126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28985626..28991343hg38UCSC Ensembl
chr11:29007173..29012890hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg385718
hg195718
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455062
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853191
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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