A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5505774



Internal ID282540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6950500..6975000hg38UCSC Ensembl
chr11:6971731..6996231hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3824501
hg1924501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041737
Samples
Known GenesZNF215
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5505774
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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