A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615832



Internal ID16403241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134654115..134655122hg38UCSC Ensembl
Innerchr9:137545961..137546968hg19UCSC Ensembl
Innerchr9:136685782..136686789hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381008
hg191008
hg181008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12977n54
Supporting Variantsnssv1146776
Samples
Known GenesCOL5A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615832
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