A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3853057



Internal ID11908814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13675115..13675299hg38UCSC Ensembl
chr18:13675114..13675298hg19UCSC Ensembl
chr18:13665114..13665298hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38185
hg19185
hg18185
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1105405
Supporting Variants
SamplesHuRef
Known GenesFAM210A
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3853057
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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