A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5512529



Internal ID289080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33905615..33908823hg38UCSC Ensembl
chr11:33927162..33930370hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383209
hg193209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5512529
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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