A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475131



Internal ID22533026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55456804..55460703hg38UCSC Ensembl
chr17:53534165..53538064hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5883761
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475131
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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