A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855950



Internal ID22630885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64328506..64330712hg38UCSC Ensembl
chr11:64095978..64098184hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382207
hg192207
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455582, nssv17455910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855950
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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