A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669519



Internal ID21617824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62349826..62349826hg38UCSC Ensembl
chr20:60924882..60924882hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117423, nssv17117246
SamplesHG02492, HG00512
Known GenesLAMA5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669519
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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