A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837829



Internal ID22612764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109583239..109626990hg38UCSC Ensembl
chr4:110504395..110548146hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3843752
hg1943752
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498194
Samples
Known GenesCCDC109B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837829
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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