A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047743



Internal ID18790274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46440224..46606240hg38UCSC Ensembl
Innerchr10:46943377..47109535hg19UCSC Ensembl
Innerchr10:46363383..46529541hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38166017
hg19166159
hg18166159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv764n100
Supporting Variantsnssv3514250
Samples
Known GenesGPRIN2, LINC00842, LOC100996758, NPY4R, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047743
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