A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041317



Internal ID18783848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46407438..46586017hg38UCSC Ensembl
Innerchr10:46963600..47142310hg19UCSC Ensembl
Innerchr10:46383606..46562316hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38178580
hg19178711
hg18178711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv764n100
Supporting Variantsnssv3709063
Samples
Known GenesGPRIN2, HNRNPA1P33, 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)nsv1041317
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