A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475809



Internal ID22533707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65631488..65632487hg38UCSC Ensembl
chr17:63627606..63628605hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475809
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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