A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3576934



Internal ID18875215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:6422361..6483245hg38UCSC Ensembl
Innerchr2:6562493..6623377hg19UCSC Ensembl
Innerchr2:6479944..6540828hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3860885
hg1960885
hg1860885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004639
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)nssv3576934
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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