A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479479



Internal ID22537381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78730568..78731694hg38UCSC Ensembl
chr17:76726650..76727776hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381127
hg191127
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875120
Supporting Variants
Samples
Known GenesCYTH1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479479
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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