A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3497798



Internal ID19085439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4244688..4264832hg38UCSC Ensembl
Innerchr10:4286880..4307024hg19UCSC Ensembl
Innerchr10:4276880..4297024hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3820145
hg1920145
hg1820145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052378
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)nssv3497798
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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