A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696248



Internal ID18647843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69475890..69503518hg38UCSC Ensembl
Innerchr9:72090806..72118434hg19UCSC Ensembl
Innerchr9:71280626..71308254hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3827629
hg1927629
hg1827629
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041401
Supporting Variants
Samples
Known GenesAPBA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696248
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