A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011462



Internal ID18753996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:179147966..179159155hg38UCSC Ensembl
Innerchr1:179117101..179128290hg19UCSC Ensembl
Innerchr1:177383724..177394913hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3811190
hg1911190
hg1811190
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv470n100
Supporting Variantsnssv3493745, nssv3493951
Samples
Known GenesABL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011462
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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