A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668338



Internal ID21616643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57618042..57618042hg38UCSC Ensembl
chr20:56193098..56193098hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117472
SamplesHG03009
Known GenesZBP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668338
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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