A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615572



Internal ID16056295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132183292..132251071hg38UCSC Ensembl
Innerchr9:135058679..135126458hg19UCSC Ensembl
Innerchr9:134048500..134116279hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3867780
hg1967780
hg1867780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1145326
Samples
Known GenesNTNG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615572
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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