A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549430



Internal ID16336839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:238897660..238927640hg38UCSC Ensembl
Innerchr1:239060960..239090940hg19UCSC Ensembl
Innerchr1:237127583..237157563hg18UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3829981
hg1929981
hg1829981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv870n54
Supporting Variantsnssv1174071
SamplesHGDP00326
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549430
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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