A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549097



Internal ID16336506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:208608141..208808979hg38UCSC Ensembl
Innerchr1:208781486..208982324hg19UCSC Ensembl
Innerchr1:206848109..207048947hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38200839
hg19200839
hg18200839
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv736032
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549097
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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