A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981895



Internal ID12974105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1713346..1863988hg38UCSC Ensembl
Innerchr18:1713347..1863989hg19UCSC Ensembl
Innerchr18:1703347..1853989hg18UCSC Ensembl
Innerchr18:1703347..1853989hg17UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38150643
hg19150643
hg18150643
hg17150643
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)essv6981895
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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