A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876740



Internal ID22651701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30185401..30190927hg38UCSC Ensembl
chr19:30676308..30681834hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg385527
hg195527
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474661
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876740
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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