A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582826



Internal ID18881107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:146085671..146109354hg38UCSC Ensembl
Innerchr2:146843239..146866922hg19UCSC Ensembl
Innerchr2:146559709..146583392hg18UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3823684
hg1923684
hg1823684
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007357
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)nssv3582826
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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