A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2935613



Internal ID15338168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:666357..666481hg38UCSC Ensembl
Innerchr6:666357..666481hg19UCSC Ensembl
Innerchr6:611357..611481hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38125
hg19125
hg18125
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514341
Supporting Variants
SamplesNA18608
Known GenesEXOC2
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2935613
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