A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947092



Internal ID22722593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71833010..71837063hg38UCSC Ensembl
chr17:69829151..69833204hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg384054
hg194054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947092
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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