A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475219



Internal ID22533114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61081493..61119354hg38UCSC Ensembl
chr17:59158854..59196715hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3837862
hg1937862
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870265
Supporting Variants
Samples
Known GenesBCAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475219
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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