A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578557



Internal ID16019280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8390530..8391108hg38UCSC Ensembl
Innerchr19:8455414..8455992hg19UCSC Ensembl
Innerchr19:8361414..8361992hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38579
hg19579
hg18579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6257n54
Supporting Variantsnssv893403
Samples
Known GenesRAB11B, RAB11B-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578557
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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