A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999873



Internal ID19159409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:113297729..113406831hg38UCSC Ensembl
Innerchr1:113840351..113949453hg19UCSC Ensembl
Innerchr1:113641874..113750976hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38109103
hg19109103
hg18109103
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv291n100
Supporting Variantsnssv3483845
Samples
Known GenesMAGI3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999873
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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