A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv763032



Internal ID16056988
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 StatusS
Merged Variantsnsv552757
Supporting Variants
Samples
Known GenesLOC653486, SCGB1C1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv763032
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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