A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862600



Internal ID22637535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9321861..9325431hg38UCSC Ensembl
chr11:9343408..9346978hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383571
hg193571
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468463
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862600
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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