A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012103



Internal ID19101321
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 StatusM
Merged Variantsdgv3994n100
Supporting Variantsnssv3579450
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)nsv1012103
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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