A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3521974



Internal ID18473569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46428386..46469221hg38UCSC Ensembl
Innerchr10:47080230..47121369hg19UCSC Ensembl
Innerchr10:46500236..46541375hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3840836
hg1941140
hg1841140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052022
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)nssv3521974
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