A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043173



Internal ID18785704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46428386..46472778hg38UCSC Ensembl
Innerchr10:47076675..47121369hg19UCSC Ensembl
Innerchr10:46496681..46541375hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3844393
hg1944695
hg1844695
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514865
Samples
Known GenesLINC00842, 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)nsv1043173
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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