A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849492



Internal ID22624427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38937219..38985917hg38UCSC Ensembl
chr11:38958769..39007467hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3848699
hg1948699
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849492
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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