A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050878



Internal ID19140097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37746263..37829965hg38UCSC Ensembl
Innerchr11:37767813..37851515hg19UCSC Ensembl
Innerchr11:37724389..37808091hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3883703
hg1983703
hg1883703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1101n100
Supporting Variantsnssv3517722, nssv3512446
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)nsv1050878
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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