A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639314



Internal ID21587619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154225744..154225744hg38UCSC Ensembl
chr5:153605304..153605304hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124965
SamplesHG00731
Known GenesGALNT10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639314
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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