A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3514594



Internal ID18812875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:107361674..107372782hg38UCSC Ensembl
Innerchr10:109121432..109132540hg19UCSC Ensembl
Innerchr10:109111422..109122530hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3811109
hg1911109
hg1811109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052074
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)nssv3514594
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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