A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1520737



Internal ID12337173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:107026152..107026152hg38UCSC Ensembl
chr12:107419930..107419930hg19UCSC Ensembl
chr12:105944060..105944060hg18UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3871
hg1971
hg1871
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4267834
SamplesHuRef
Known GenesCRY1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1520737
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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