A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933658



Internal ID22708972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8415210..8415465hg38UCSC Ensembl
chr17:8318528..8318783hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381112
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933658
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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