A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3468189



Internal ID19062713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:101895054..101962788hg38UCSC Ensembl
Innerchr1:102360610..102428344hg19UCSC Ensembl
Innerchr1:102133198..102200932hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3867735
hg1967735
hg1867735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004240
Supporting Variants
Samples
Known GenesMIR548AI, OLFM3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3468189
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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