A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548861



Internal ID16336270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196856498..196925196hg38UCSC Ensembl
Innerchr1:196825628..196894326hg19UCSC Ensembl
Innerchr1:195092251..195160949hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3868699
hg1968699
hg1868699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv753n54
Supporting Variantsnssv1174027
SamplesHGDP01094
Known GenesCFHR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548861
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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