A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048624



Internal ID18791155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90100568..91604298hg38UCSC Ensembl
Innerchr11:89833736..91337464hg19UCSC Ensembl
Innerchr11:89473384..90977112hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg381503731
hg191503729
hg181503729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518304
Samples
Known GenesCHORDC1, DISC1FP1, MIR4490, NAALAD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048624
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