A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5504978



Internal ID281768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32887581..32887674hg38UCSC Ensembl
chr11:32909127..32909220hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043104
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5504978
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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