A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002773



Internal ID18745305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65724045..65899988hg38UCSC Ensembl
Innerchr3:65709720..65885663hg19UCSC Ensembl
Innerchr3:65684760..65860703hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38175944
hg19175944
hg18175944
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4769n100
Supporting Variantsnssv3593957
Samples
Known GenesMAGI1, MAGI1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002773
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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