A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2937452



Internal ID15802835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:39101122..39104278hg38UCSC Ensembl
Innerchr6:39068898..39072054hg19UCSC Ensembl
Innerchr6:39176876..39180032hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg383157
hg193157
hg183157
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514357
Supporting Variants
SamplesNA21523
Known GenesSAYSD1
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2937452
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