A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579887



Internal ID16367296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46190005..46279349hg38UCSC Ensembl
Innerchr19:46693262..46782606hg19UCSC Ensembl
Innerchr19:51385102..51474446hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3889345
hg1989345
hg1889345
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150649
SamplesNINDS_133
Known GenesDKFZp434J0226, IGFL1, RNU6-66P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579887
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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