A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv971263



Internal ID16265219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:105214314..105277908hg38UCSC Ensembl
Innerchr3:104933158..104996752hg19UCSC Ensembl
Innerchr3:106415848..106479442hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3863595
hg1963595
hg1863595
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591239
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv971263
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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