A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3507908



Internal ID18806189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:107372533..107396152hg38UCSC Ensembl
Innerchr10:109132291..109155910hg19UCSC Ensembl
Innerchr10:109122281..109145900hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3823620
hg1923620
hg1823620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041790
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)nssv3507908
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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