A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615311



Internal ID16402720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126496558..126519369hg38UCSC Ensembl
Innerchr9:129258837..129281648hg19UCSC Ensembl
Innerchr9:128298658..128321469hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3822812
hg1922812
hg1822812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176494
SamplesNINDS_49
Known GenesMVB12B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615311
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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