A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929303



Internal ID22704554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81805610..81805706hg38UCSC Ensembl
chr17:79763486..79763582hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389435
Samples
Known GenesGCGR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929303
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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