A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169898



Internal ID21313709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:102951134..103038606hg38UCSC Ensembl
Outerchr1:102946505..103044702hg38UCSC Ensembl
Innerchr1:103416690..103504162hg19UCSC Ensembl
Outerchr1:103412061..103510258hg19UCSC Ensembl
Innerchr1:103189278..103276750hg18UCSC Ensembl
Outerchr1:103184649..103282846hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3898198
hg1998198
hg1898198
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242317, nssv14249343
SamplesNGO_22, NGO_24
Known GenesCOL11A1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169898
Frequency
Sample Size93
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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