A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007610



Internal ID19096829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14210406..14279948hg38UCSC Ensembl
Innerchr3:14251906..14321448hg19UCSC Ensembl
Innerchr3:14226910..14296452hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3869543
hg1969543
hg1869543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593088
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)nsv1007610
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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