A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831056



Internal ID22605991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:99281295..99282740hg38UCSC Ensembl
chr1:99746851..99748296hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg381446
hg191446
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482536
Samples
Known GenesLPPR4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831056
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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