A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999890



Internal ID19159426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88861741..89245848hg38UCSC Ensembl
Innerchr2:89161253..89545331hg19UCSC Ensembl
Innerchr2:88942368..89326446hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38384108
hg19384079
hg18384079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3926n100
Supporting Variantsnssv3729890, nssv3729889
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999890
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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