A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504905



Internal ID18456500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14305146..14338953hg38UCSC Ensembl
Innerchr10:14347145..14380952hg19UCSC Ensembl
Innerchr10:14387151..14420958hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3833808
hg1933808
hg1833808
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037322
Supporting Variants
Samples
Known GenesFRMD4A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3504905
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