A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697608



Internal ID18995889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103265259..103290151hg38UCSC Ensembl
Innerchr9:106027541..106052433hg19UCSC Ensembl
Innerchr9:105067362..105092254hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3824893
hg1924893
hg1824893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043051
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)nssv3697608
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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