A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839070



Internal ID22614005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53204195..53218918hg38UCSC Ensembl
chr4:54070362..54085085hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3814724
hg1914724
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495918
Samples
Known GenesSCFD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839070
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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