A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011853



Internal ID18754388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:93500893..93573448hg38UCSC Ensembl
Innerchr1:93966450..94039005hg19UCSC Ensembl
Innerchr1:93739038..93811593hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg3872556
hg1972556
hg1872556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3699601
Samples
Known GenesBCAR3, FNBP1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011853
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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