A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3915524



Internal ID11499661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132069343..132069707hg38UCSC Ensembl
chr11:131939237..131939601hg19UCSC Ensembl
chr11:131444447..131444811hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38365
hg19365
hg18365
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1186595
Supporting Variants
SamplesHuRef
Known GenesNTM
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3915524
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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