A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504218



Internal ID18802499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:106047073..106551938hg38UCSC Ensembl
Innerchr10:107806831..108311696hg19UCSC Ensembl
Innerchr10:107796821..108301686hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38504866
hg19504866
hg18504866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036619
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3504218
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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