A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865991



Internal ID22640926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34135927..34137026hg38UCSC Ensembl
chr11:34157474..34158573hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464953, nssv17451573
Samples
Known GenesNAT10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865991
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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