A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615979



Internal ID16056702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136624266..136688703hg38UCSC Ensembl
Innerchr9:139518718..139583155hg19UCSC Ensembl
Innerchr9:138638539..138702976hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3864438
hg1964438
hg1864438
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv13005n54
Supporting Variantsnssv1148333
Samples
Known GenesAGPAT2, EGFL7, MIR126
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615979
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