A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847896



Internal ID22622831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88357487..88358624hg38UCSC Ensembl
chr11:88090655..88091792hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg381138
hg191138
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463081, nssv17455408
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847896
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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