A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3577037



Internal ID18875318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13064541..13139143hg38UCSC Ensembl
Innerchr2:13204666..13279268hg19UCSC Ensembl
Innerchr2:13122117..13196719hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3874603
hg1974603
hg1874603
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009836
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)nssv3577037
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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