A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500667



Internal ID277595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60397729..60398348hg38UCSC Ensembl
chr11:60165202..60165821hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047806
Samples
Known GenesMS4A14
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500667
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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