A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999432



Internal ID18812282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100621212..100729339hg38UCSC Ensembl
Innerchr3:100340056..100448183hg19UCSC Ensembl
Innerchr3:101822746..101930873hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38108128
hg19108128
hg18108128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4830n100
Supporting Variantsnssv3604348, nssv3604347
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)nsv999432
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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