A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003890



Internal ID19093108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89928002..90077966hg38UCSC Ensembl
Innerchr2:89966812..90116808hg19UCSC Ensembl
Innerchr2:89604119..89754113hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38149965
hg19149997
hg18149995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3973n100
Supporting Variantsnssv3580454
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)nsv1003890
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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