A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3474531



Internal ID19066026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:101895054..101972876hg38UCSC Ensembl
Innerchr1:102360610..102438432hg19UCSC Ensembl
Innerchr1:102133198..102211020hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3877823
hg1977823
hg1877823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012856
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)nssv3474531
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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