A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615982



Internal ID16403391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136752622..136799540hg38UCSC Ensembl
Innerchr9:139647074..139693992hg19UCSC Ensembl
Innerchr9:138766895..138813813hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3846919
hg1946919
hg1846919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176165
Samples1780862197_A
Known GenesCCDC183, LCN15, LCN8, TMEM141
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615982
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