A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026175



Internal ID18768707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189903701..190052393hg38UCSC Ensembl
Innerchr4:190824856..190973548hg19UCSC Ensembl
Innerchr4:191061850..191210542hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38148693
hg19148693
hg18148693
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5507n100
Supporting Variantsnssv3744567, nssv3744566
Samples
Known GenesFRG1, FRG2, LOC100288255, LOC283788
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026175
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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