A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584101



Internal ID16371510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:194382880..194488162hg38UCSC Ensembl
Innerchr2:195247604..195352886hg19UCSC Ensembl
Innerchr2:194955849..195061131hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38105283
hg19105283
hg18105283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7240n54
Supporting Variantsnssv930171, nssv930170
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584101
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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