A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581862



Internal ID16022585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:50850431..51108720hg38UCSC Ensembl
Innerchr2:51077569..51335858hg19UCSC Ensembl
Innerchr2:50931073..51189362hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38258290
hg19258290
hg18258290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6866n54
Supporting Variantsnssv908382
Samples
Known GenesNRXN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581862
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer