A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690663



Internal ID18988944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17590301..17632545hg38UCSC Ensembl
Innerchr9:17590299..17632543hg19UCSC Ensembl
Innerchr9:17580299..17622543hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3842245
hg1942245
hg1842245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024129
Supporting Variants
Samples
Known GenesSH3GL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690663
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