A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987378



Internal ID12981841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71910057..72220902hg38UCSC Ensembl
Innerchr18:69577293..69888137hg19UCSC Ensembl
Innerchr18:67728273..68039117hg18UCSC Ensembl
Innerchr18:67728273..68039117hg17UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38310846
hg19310845
hg18310845
hg17310845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35041
Supporting Variants
SamplesNA19007
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987378
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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