A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006160



Internal ID19095378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:102190625..102376359hg38UCSC Ensembl
Innerchr1:102656181..102841915hg19UCSC Ensembl
Innerchr1:102428769..102614503hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38185735
hg19185735
hg18185735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv210n100
Supporting Variantsnssv3466696
Samples
Known GenesMIR548AI
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006160
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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