A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555628



Internal ID16343037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84977018..84980946hg38UCSC Ensembl
Innerchr11:84688062..84691990hg19UCSC Ensembl
Innerchr11:84365710..84369638hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg383929
hg193929
hg183929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv779867
Samples
Known GenesDLG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555628
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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