A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830236



Internal ID22605171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50035460..50057135hg38UCSC Ensembl
chr1:50501132..50522807hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3821676
hg1921676
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480068
Samples
Known GenesELAVL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830236
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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