A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052258



Internal ID19141477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50337834..50810134hg38UCSC Ensembl
Innerchr11:50297005..50769305hg19UCSC Ensembl
Innerchr11:50253581..50725881hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38472301
hg19472301
hg18472301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1141n100
Supporting Variantsnssv3519091
Samples
Known GenesLOC646813
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052258
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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