A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014057



Internal ID18756589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8783669..8825505hg38UCSC Ensembl
Innerchr3:8825355..8867190hg19UCSC Ensembl
Innerchr3:8800355..8842190hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3841837
hg1941836
hg1841836
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4679n100
Supporting Variantsnssv3739630, nssv3739632, nssv3739631, nssv3591924
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)nsv1014057
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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