A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507797



Internal ID284507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31850228..31878569hg38UCSC Ensembl
chr11:31871774..31900115hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3828342
hg1928342
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044620
Samples
Known GenesDKFZp686K1684
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507797
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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