A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969602



Internal ID22744537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131454729..131454729hg38UCSC Ensembl
chr11:131324623..131324623hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358571
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969602
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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