A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695169



Internal ID18646764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116639065..116863135hg38UCSC Ensembl
Innerchr9:119401344..119625414hg19UCSC Ensembl
Innerchr9:118441165..118665235hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38224071
hg19224071
hg18224071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047284
Supporting Variants
Samples
Known GenesASTN2, TRIM32
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695169
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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