A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828062



Internal ID22602997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161016757..161029554hg38UCSC Ensembl
chr1:160986547..160999344hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3812798
hg1912798
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451806
Samples
Known GenesF11R
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828062
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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