A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921598



Internal ID22696822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101964045..101964371hg38UCSC Ensembl
chr11:101834776..101835102hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367789
Samples
Known GenesKIAA1377
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921598
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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