A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006402



Internal ID18748933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100621212..100728122hg38UCSC Ensembl
Innerchr3:100340056..100446966hg19UCSC Ensembl
Innerchr3:101822746..101929656hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38106911
hg19106911
hg18106911
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4830n100
Supporting Variantsnssv3604341, nssv3735233, nssv3604343, nssv3604342, nssv3604346, nssv3604340, nssv3604344, nssv3604345
Samples
Known GenesGPR128, TFG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006402
Frequency
Sample Size29084
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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