A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044698



Internal ID19133917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119896905..119918974hg38UCSC Ensembl
Innerchr11:119767614..119789683hg19UCSC Ensembl
Innerchr11:119272824..119294893hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3822070
hg1922070
hg1822070
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1285n100
Supporting Variantsnssv3516366
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)nsv1044698
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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