A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037170



Internal ID19126389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:87830530..87964554hg38UCSC Ensembl
Innerchr11:87541422..87675446hg19UCSC Ensembl
Innerchr11:87219070..87353094hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38134025
hg19134025
hg18134025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504763
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)nsv1037170
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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