A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051992



Internal ID18794523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46407438..46588039hg38UCSC Ensembl
Innerchr10:46961578..47142310hg19UCSC Ensembl
Innerchr10:46381584..46562316hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38180602
hg19180733
hg18180733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv764n100
Supporting Variantsnssv3709062
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)nsv1051992
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