A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013792



Internal ID18756324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3005296..3391724hg38UCSC Ensembl
Innerchr1:2921860..3308288hg19UCSC Ensembl
Innerchr1:2911720..3298148hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38386429
hg19386429
hg18386429
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3477002
Samples
Known GenesACTRT2, LINC00982, MIR4251, PRDM16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013792
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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