A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944320



Internal ID22719783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5906651..6017279hg38UCSC Ensembl
chr17:5809971..5920599hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38110629
hg19110629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383228
Samples
Known GenesLOC339166
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944320
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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