A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829835



Internal ID22604770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32500798..32503797hg38UCSC Ensembl
chr1:32966399..32969398hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv37n209
Supporting Variantsnssv17460243
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829835
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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