A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580872



Internal ID16368281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:5705411..5710632hg38UCSC Ensembl
Innerchr2:5845543..5850764hg19UCSC Ensembl
Innerchr2:5762994..5768215hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg385222
hg195222
hg185222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6675n54
Supporting Variantsnssv903361
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580872
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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