A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010228



Internal ID18752759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:2777886..3350773hg38UCSC Ensembl
Innerchr1:2694433..3267337hg19UCSC Ensembl
Innerchr1:2684293..3257197hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38572888
hg19572905
hg18572905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11n100
Supporting Variantsnssv3470582
Samples
Known GenesACTRT2, LINC00982, MIR4251, PRDM16, TTC34
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010228
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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