A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv970686



Internal ID15917956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100616244..100726010hg38UCSC Ensembl
Innerchr3:100335088..100444854hg19UCSC Ensembl
Innerchr3:101817778..101927544hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38109767
hg19109767
hg18109767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591155
Supporting Variants
Samples
Known GenesGPR128, TFG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv970686
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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