A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014836



Internal ID19104053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:105426670..105544653hg38UCSC Ensembl
Innerchr1:105969292..106087275hg19UCSC Ensembl
Innerchr1:105770815..105888798hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38117984
hg19117984
hg18117984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv236n100
Supporting Variantsnssv3498143
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014836
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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