A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2970634



Internal ID15680122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130268868..130270228hg38UCSC Ensembl
Innerchr9:133031147..133032507hg19UCSC Ensembl
Innerchr9:132070968..132072328hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381361
hg191361
hg181361
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515127
Supporting Variants
SamplesNA18572
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2970634
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer