A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579450



Internal ID18877731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91460974..91601674hg38UCSC Ensembl
Innerchr2:91653350..91789700hg19UCSC Ensembl
Innerchr2:91017077..91153427hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38140701
hg19136351
hg18136351
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012103
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)nssv3579450
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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