A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495649



Internal ID22553582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143104005..143107449hg38UCSC Ensembl
chr5:142483570..142487014hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg383445
hg193445
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841165
Supporting Variants
Samples
Known GenesARHGAP26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495649
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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