A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857750



Internal ID22632685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18465855..18486313hg38UCSC Ensembl
chr11:18487402..18507860hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3820459
hg1920459
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454710
Samples
Known GenesLDHAL6A, TSG101
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857750
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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