A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3572076



Internal ID7043458
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 StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1000221
Supporting Variants
SamplesHuRef
Known GenesANKRD28
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3572076
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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