A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989538



Internal ID12974097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1735367..1825169hg38UCSC Ensembl
Innerchr18:1735368..1825170hg19UCSC Ensembl
Innerchr18:1725368..1815170hg18UCSC Ensembl
Innerchr18:1725368..1815170hg17UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3889803
hg1989803
hg1889803
hg1789803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751772
Supporting Variants
SamplesBEC_5
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989538
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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