A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143327



Internal ID342528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:980044..980541hg38UCSC Ensembl
chr11:980044..980541hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041970
Samples
Known GenesAP2A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143327
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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