A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3937288



Internal ID11477898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3833187..3833239hg38UCSC Ensembl
chr18:3833187..3833239hg19UCSC Ensembl
chr18:3823187..3823239hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3853
hg1953
hg1853
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1733623
Supporting Variants
SamplesHuRef
Known GenesDLGAP1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3937288
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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