A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1681196



Internal ID12497628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12691364..12691432hg38UCSC Ensembl
chr10:12733363..12733431hg19UCSC Ensembl
chr10:12773369..12773437hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3869
hg1969
hg1869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3900741
SamplesHuRef
Known GenesCAMK1D
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1681196
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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