A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938169



Internal ID22713547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4955807..4955883hg38UCSC Ensembl
chr17:4859102..4859178hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378370
Samples
Known GenesENO3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938169
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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