A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1053603



Internal ID11870042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3674895..3675033hg38UCSC Ensembl
chr18:3674895..3675033hg19UCSC Ensembl
chr18:3664895..3665033hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38139
hg19139
hg18139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4217052
SamplesHuRef
Known GenesDLGAP1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1053603
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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