A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004611



Internal ID19093828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:166067622..166226838hg38UCSC Ensembl
Innerchr3:165785410..165944626hg19UCSC Ensembl
Innerchr3:167268104..167427320hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38159217
hg19159217
hg18159217
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4980n100
Supporting Variantsnssv3738318, nssv3738319, nssv3612689
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)nsv1004611
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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