A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828895



Internal ID22603830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21785134..21789149hg38UCSC Ensembl
chr1:22111627..22115642hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg384016
hg194016
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466791
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828895
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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