A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696224



Internal ID18647819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69071560..69103531hg38UCSC Ensembl
Innerchr9:71686476..71718447hg19UCSC Ensembl
Innerchr9:70876296..70908267hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3831972
hg1931972
hg1831972
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042844
Supporting Variants
Samples
Known GenesFXN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696224
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