A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695572



Internal ID18647167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61983603hg38UCSC Ensembl
Innerchr9:44727847..45119755hg19UCSC Ensembl
Innerchr9:44667843..45059751hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38463595
hg19391909
hg18391909
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028842
Supporting Variants
Samples
Known GenesFAM27C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695572
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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