A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3466542



Internal ID19061811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:102190625..102378068hg38UCSC Ensembl
Innerchr1:102656181..102843624hg19UCSC Ensembl
Innerchr1:102428769..102616212hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38187444
hg19187444
hg18187444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003711
Supporting Variants
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)nssv3466542
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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