A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv712950



Internal ID15660220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:47416966..47423745hg38UCSC Ensembl
Innerchr1:47882638..47889417hg19UCSC Ensembl
Innerchr1:47655225..47662004hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg386780
hg196780
hg186780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546184
Supporting Variants
Samples
Known GenesFOXE3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv712950
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