A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057355



Internal ID19146574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:29250385..29364572hg38UCSC Ensembl
Innerchr18:26830350..26944537hg19UCSC Ensembl
Innerchr18:25084348..25198535hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38114188
hg19114188
hg18114188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725303
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)nsv1057355
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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