A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056587



Internal ID19145806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:29259820..30263106hg38UCSC Ensembl
Innerchr18:26839785..27843071hg19UCSC Ensembl
Innerchr18:25093783..26097069hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381003287
hg191003287
hg181003287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564149
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)nsv1056587
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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