A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864069



Internal ID22639004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76961516..76965814hg38UCSC Ensembl
chr11:76672560..76676858hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg384299
hg194299
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455684
Samples
Known GenesACER3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864069
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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