A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045523



Internal ID19134742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24167219..24214550hg38UCSC Ensembl
Innerchr11:24188765..24236096hg19UCSC Ensembl
Innerchr11:24145341..24192672hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3847332
hg1947332
hg1847332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3515305
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)nsv1045523
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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