A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755818



Internal ID20531678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56635262..56635262hg38UCSC Ensembl
chr19:57146630..57146630hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262782
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755818
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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