A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1542857



Internal ID12359292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:18369826..18369976hg38UCSC Ensembl
chr12:18522760..18522910hg19UCSC Ensembl
chr12:18414027..18414177hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38151
hg19151
hg18151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4310709
SamplesHuRef
Known GenesPIK3C2G
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1542857
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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