A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007799



Internal ID19097018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..86250hg38UCSC Ensembl
Innerchr3:60333..127933hg19UCSC Ensembl
Innerchr3:35333..102933hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3867596
hg1967601
hg1867601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4604n100
Supporting Variantsnssv3593527
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)nsv1007799
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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