A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4170875



Internal ID11453413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2385619..2385681hg38UCSC Ensembl
chr11:2406849..2406911hg19UCSC Ensembl
chr11:2363425..2363487hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3863
hg1963
hg1863
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1285833
Supporting Variants
SamplesHuRef
Known GenesCD81
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4170875
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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