A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475153



Internal ID22533048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5780827..5781919hg38UCSC Ensembl
chr17:5684147..5685239hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg381093
hg191093
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882385
Supporting Variants
Samples
Known GenesLOC339166
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475153
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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