A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968044



Internal ID22742979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24575756..24575756hg38UCSC Ensembl
chr16:24587077..24587077hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380985
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968044
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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