A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614954



Internal ID16402363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:99026240..99054117hg38UCSC Ensembl
Innerchr9:101788522..101816399hg19UCSC Ensembl
Innerchr9:100828343..100856220hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3827878
hg1927878
hg1827878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176003
SamplesNINDS_198
Known GenesCOL15A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614954
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