A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1211696



Internal ID12374820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165826368..165826417hg38UCSC Ensembl
chr6:166239856..166239905hg19UCSC Ensembl
chr6:166159846..166159895hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3656531
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1211696
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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