A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933689



Internal ID22709003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34993209..34994147hg38UCSC Ensembl
chr17:33320228..33321166hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38939
hg19939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387005
Samples
Known GenesLIG3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933689
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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