A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555632



Internal ID15996355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85684137..85725309hg38UCSC Ensembl
Innerchr11:85395180..85436352hg19UCSC Ensembl
Innerchr11:85072828..85114000hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3841173
hg1941173
hg1841173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176188
Samples1780862596_A
Known GenesCCDC89, SYTL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555632
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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