A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969894



Internal ID22744829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20062001..20062001hg38UCSC Ensembl
chr11:20083547..20083547hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351287
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969894
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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