A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141313



Internal ID15647813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:123365719..123425419hg38UCSC Ensembl
Innerchr9:126127998..126187698hg19UCSC Ensembl
Innerchr9:125167819..125227519hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3859701
hg1959701
hg1859701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615285
Supporting Variants
Samples
Known GenesCRB2, DENND1A, MIR601
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141313
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