A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014757



Internal ID19103974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:113318902..113426795hg38UCSC Ensembl
Innerchr1:113861524..113969417hg19UCSC Ensembl
Innerchr1:113663047..113770940hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38107894
hg19107894
hg18107894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv291n100
Supporting Variantsnssv3498061
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)nsv1014757
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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