A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1611893



Internal ID12775013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19859893..19860067hg38UCSC Ensembl
chr11:19881439..19881613hg19UCSC Ensembl
chr11:19838015..19838189hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38175
hg19175
hg18175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587632
SamplesHuRef
Known GenesNAV2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1611893
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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