A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047169



Internal ID19136388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71342252..71384345hg38UCSC Ensembl
Innerchr11:71053298..71095391hg19UCSC Ensembl
Innerchr11:70730946..70773039hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3842094
hg1942094
hg1842094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710640
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)nsv1047169
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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