A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549095



Internal ID16336504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:208365486..208945441hg38UCSC Ensembl
Innerchr1:208538831..209118786hg19UCSC Ensembl
Innerchr1:206605454..207185409hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38579956
hg19579956
hg18579956
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv736030
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549095
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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