A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581859



Internal ID16022582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:50820175..51053379hg38UCSC Ensembl
Innerchr2:51047313..51280517hg19UCSC Ensembl
Innerchr2:50900817..51134021hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38233205
hg19233205
hg18233205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6866n54
Supporting Variantsnssv908379
Samples
Known GenesNRXN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581859
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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