A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584754



Internal ID16025477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:237865062..237894836hg38UCSC Ensembl
Innerchr2:238773705..238803478hg19UCSC Ensembl
Innerchr2:238438444..238468217hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3829775
hg1929774
hg1829774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv933708
Samples
Known GenesRAMP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584754
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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