A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3507598



Internal ID18805879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26936975..26955043hg38UCSC Ensembl
Innerchr10:27225904..27243972hg19UCSC Ensembl
Innerchr10:27265910..27283978hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3818069
hg1918069
hg1818069
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036722
Supporting Variants
Samples
Known GenesLINC00202-1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3507598
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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