A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105270



Internal ID22014503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35806942..35806942hg38UCSC Ensembl
chr19:36297844..36297844hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636408
Samples
Known GenesPRODH2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105270
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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