A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509565



Internal ID18807846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50019689..50152081hg38UCSC Ensembl
Innerchr10:51779449..51911841hg19UCSC Ensembl
Innerchr10:51449455..51581847hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38132393
hg19132393
hg18132393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039808
Supporting Variants
Samples
Known GenesFAM21A, FAM21B, FLJ31813
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3509565
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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