A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492239



Internal ID22550166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108997400..109040932hg38UCSC Ensembl
chr4:109918556..109962088hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3843533
hg1943533
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836963
Supporting Variants
Samples
Known GenesCOL25A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492239
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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