A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997532



Internal ID19157068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103058357..103092660hg38UCSC Ensembl
Innerchr3:102777201..102811504hg19UCSC Ensembl
Innerchr3:104259891..104294194hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3834304
hg1934304
hg1834304
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604375
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)nsv997532
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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