A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1015874



Internal ID11832314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:20623628..20623682hg38UCSC Ensembl
chr12:20776562..20776616hg19UCSC Ensembl
chr12:20667829..20667883hg18UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg3855
hg1955
hg1855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3798946
SamplesHuRef
Known GenesPDE3A
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1015874
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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