A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869650



Internal ID22644585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44667511..44670143hg38UCSC Ensembl
chr19:45170779..45173415hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg382633
hg192637
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476706, nssv17476705
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869650
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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