A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972304



Internal ID22747239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43794420..43794420hg38UCSC Ensembl
chr19:44298572..44298572hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402634
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972304
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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