A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555404



Internal ID15996127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:72233198..72238908hg38UCSC Ensembl
Innerchr11:71944242..71949952hg19UCSC Ensembl
Innerchr11:71621890..71627600hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg385711
hg195711
hg185711
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv778988, nssv778987
Samples
Known GenesINPPL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555404
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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