A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830817



Internal ID22605752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:934914..944012hg38UCSC Ensembl
chr1:870294..879392hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg389099
hg199099
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482484
Samples
Known GenesSAMD11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830817
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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