A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000221



Internal ID7065356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15737521..15737522hg38UCSC Ensembl
chr3:15779028..15779029hg19UCSC Ensembl
chr3:15754032..15754033hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38144
hg19144
hg18144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3572076
SamplesHuRef
Known GenesANKRD28
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000221
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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