A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049356



Internal ID18791887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132170367..132210675hg38UCSC Ensembl
Innerchr9:135045754..135086062hg19UCSC Ensembl
Innerchr9:134035575..134075883hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3840309
hg1940309
hg1840309
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696400
Samples
Known GenesNTNG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049356
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