A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv720219



Internal ID16014175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:104850325..104881533hg38UCSC Ensembl
Innerchr1:105392947..105424155hg19UCSC Ensembl
Innerchr1:105194470..105225678hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3831209
hg1931209
hg1831209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547225
Supporting Variants
Samples
Known GenesMIR548H3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv720219
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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