A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556574



Internal ID15997297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130769783..131025830hg38UCSC Ensembl
Innerchr11:130639678..130895725hg19UCSC Ensembl
Innerchr11:130144888..130400935hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38256048
hg19256048
hg18256048
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv785110
Samples
Known GenesSNX19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556574
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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