A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705127



Internal ID15095093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:121700454..121855368hg38UCSC Ensembl
Innerchr3:121419301..121574215hg19UCSC Ensembl
Innerchr3:122901991..123056905hg18UCSC Ensembl
Innerchr3:122901991..123056905hg17UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38154915
hg19154915
hg18154915
hg17154915
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516233
Supporting Variants
Samples
Known GenesEAF2, GOLGB1, IQCB1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705127
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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