A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478837



Internal ID22536739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:54955565..54957064hg38UCSC Ensembl
chr17:53032926..53034425hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5883999
Supporting Variants
Samples
Known GenesCOX11, TOM1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478837
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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