A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004659



Internal ID19093876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89200973..90224032hg38UCSC Ensembl
Innerchr2:89500461..90262898hg19UCSC Ensembl
Innerchr2:89281576..89900203hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381023060
hg19762438
hg18618628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3965n100
Supporting Variantsnssv3582505
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)nsv1004659
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