A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012385



Internal ID19101602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164051109..164113464hg38UCSC Ensembl
Innerchr3:163768897..163831252hg19UCSC Ensembl
Innerchr3:165251591..165313946hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3862356
hg1962356
hg1862356
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614534
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)nsv1012385
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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