A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049480



Internal ID19138699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71652953..71822873hg38UCSC Ensembl
Innerchr11:71363999..71533919hg19UCSC Ensembl
Innerchr11:71041647..71211567hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38169921
hg19169921
hg18169921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1223n100
Supporting Variantsnssv3516015
Samples
Known GenesALG1L9P, FAM86C1, ZNF705E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049480
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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