A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707694



Internal ID18659289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14941160..15018277hg38UCSC Ensembl
Innerchr10:14983159..15060276hg19UCSC Ensembl
Innerchr10:15023165..15100282hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3877118
hg1977118
hg1877118
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037136
Supporting Variants
Samples
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3707694
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