A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581837



Internal ID16369246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:50003196..50041478hg38UCSC Ensembl
Innerchr2:50230334..50268616hg19UCSC Ensembl
Innerchr2:50083838..50122120hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3838283
hg1938283
hg1838283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv908359
Samples
Known GenesNRXN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581837
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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