A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3743946



Internal ID18695541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68564420..68623605hg38UCSC Ensembl
Innerchr4:69430138..69489323hg19UCSC Ensembl
Innerchr4:69112733..69171918hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3859186
hg1959186
hg1859186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015130
Supporting Variants
Samples
Known GenesUGT2B17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3743946
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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