A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007953



Internal ID19097172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:55098324..55132682hg38UCSC Ensembl
Innerchr3:55132351..55166709hg19UCSC Ensembl
Innerchr3:55107391..55141749hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3834359
hg1934359
hg1834359
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593381
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)nsv1007953
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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