A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839645



Internal ID22614580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46151152..46152502hg38UCSC Ensembl
chr4:46153169..46154519hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg381351
hg191351
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839645
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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