A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511558



Internal ID18463153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46432210..46487142hg38UCSC Ensembl
Innerchr10:47062299..47117543hg19UCSC Ensembl
Innerchr10:46482305..46537549hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3854933
hg1955245
hg1855245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045044
Supporting Variants
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)nssv3511558
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