A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591164



Internal ID16378573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100631901..100748174hg38UCSC Ensembl
Innerchr3:100350745..100467018hg19UCSC Ensembl
Innerchr3:101833435..101949708hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38116274
hg19116274
hg18116274
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152017, nssv970725, nssv970726
Samples1780854568_A
Known GenesGPR128, TFG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591164
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer