A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056662



Internal ID19145881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:75367542..75382620hg38UCSC Ensembl
Innerchr18:73079497..73094575hg19UCSC Ensembl
Innerchr18:71208485..71223563hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3815079
hg1915079
hg1815079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563028
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056662
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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