A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048323



Internal ID19137542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15159377..15179614hg38UCSC Ensembl
Innerchr11:15180923..15201160hg19UCSC Ensembl
Innerchr11:15137499..15157736hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3820238
hg1920238
hg1820238
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1060n100
Supporting Variantsnssv3708517
Samples
Known GenesINSC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048323
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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