A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552757



Internal ID16340166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:174519..196425hg38UCSC Ensembl
Innerchr11:174519..196425hg19UCSC Ensembl
Innerchr11:164519..186425hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3821907
hg1921907
hg1821907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763032
Samples
Known GenesLOC653486, SCGB1C1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552757
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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