A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020038



Internal ID19109257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180099789..180139589hg38UCSC Ensembl
Innerchr5:179526789..179566589hg19UCSC Ensembl
Innerchr5:179459395..179499195hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3839801
hg1939801
hg1839801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3649315
Samples
Known GenesRASGEF1C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020038
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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