A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584161



Internal ID16024884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:201644883..201664791hg38UCSC Ensembl
Innerchr2:202509606..202529514hg19UCSC Ensembl
Innerchr2:202217851..202237759hg18UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3819909
hg1919909
hg1819909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7249n54
Supporting Variantsnssv930352
Samples
Known GenesMPP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584161
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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