A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471203



Internal ID21128756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93730001..93733100hg38UCSC Ensembl
chr11:93463167..93466266hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995247
Samples
Known GenesKIAA1731, SNORA1, SNORA25, SNORA32, SNORA8, SNORD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471203
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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