A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493774



Internal ID22551704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119630507..119631551hg38UCSC Ensembl
chr5:118966202..118967246hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg381045
hg191045
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841353
Supporting Variants
Samples
Known GenesFAM170A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493774
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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