A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663221



Internal ID21611526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7846996..7846996hg38UCSC Ensembl
chr19:7911882..7911882hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106885
SamplesHG01596
Known GenesEVI5L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663221
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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