A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3705759



Internal ID19004040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46989539..47108045hg19UCSC Ensembl
Innerchr10:46409545..46528051hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19118507
hg18118507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046066
Supporting Variants
Samples
Known GenesGPRIN2, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3705759
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer