A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053369



Internal ID18795900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9626290..9854507hg38UCSC Ensembl
Innerchr11:9647837..9876054hg19UCSC Ensembl
Innerchr11:9604413..9832630hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38228218
hg19228218
hg18228218
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522385
Samples
Known GenesLOC440028, SBF2, SBF2-AS1, SWAP70
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053369
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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