A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1509664



Internal ID12672786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:134237703..134237767hg38UCSC Ensembl
chr2:134995274..134995338hg19UCSC Ensembl
chr2:134711744..134711808hg18UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg3865
hg1965
hg1865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4060170
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1509664
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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