A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3787736



Internal ID11627449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14326779..14327095hg38UCSC Ensembl
chr11:14348325..14348641hg19UCSC Ensembl
chr11:14304901..14305217hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38317
hg19317
hg18317
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1753534
Supporting Variants
SamplesHuRef
Known GenesRRAS2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3787736
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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