A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006373



Internal ID18748904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100621212..100723542hg38UCSC Ensembl
Innerchr3:100340056..100442386hg19UCSC Ensembl
Innerchr3:101822746..101925076hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38102331
hg19102331
hg18102331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4830n100
Supporting Variantsnssv3604277, nssv3735208
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)nsv1006373
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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