A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587632



Internal ID12174236
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1611893
Supporting Variants
SamplesHuRef
Known GenesNAV2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3587632
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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