A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356734



Internal ID22582403
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 StatusS
Merged Variantsnsv5921823
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356734
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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