A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921823



Internal ID22697047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44254026..44254103hg38UCSC Ensembl
chr11:44275576..44275653hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921823
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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