A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983543



Internal ID12976467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1900056..2007870hg38UCSC Ensembl
Innerchr18:1900057..2007871hg19UCSC Ensembl
Innerchr18:1890057..1997871hg18UCSC Ensembl
Innerchr18:1890057..1997871hg17UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38107815
hg19107815
hg18107815
hg17107815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751775
Supporting Variants
SamplesBEC_667
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983543
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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