A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706195



Internal ID21378471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65509598..65509900hg38UCSC Ensembl
chr17:63505716..63506018hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4391853
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706195
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00574713


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