A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009768



Internal ID19098987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:95925434..95985736hg38UCSC Ensembl
Innerchr3:95644278..95704580hg19UCSC Ensembl
Innerchr3:97126968..97187270hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3860303
hg1960303
hg1860303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3603303
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)nsv1009768
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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