A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837738



Internal ID22612673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146677523..146706579hg38UCSC Ensembl
chr4:147598675..147627731hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3829057
hg1929057
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837738
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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