A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473113



Internal ID22531005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33711617..33715459hg38UCSC Ensembl
chr17:32038636..32042478hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383843
hg193843
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881738
Supporting Variants
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473113
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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