A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2940833



Internal ID15378138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143526465..143843910hg38UCSC Ensembl
Innerchr7:143223558..143541003hg19UCSC Ensembl
Innerchr7:142933680..143171936hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38317446
hg19317446
hg18238257
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514455
Supporting Variants
SamplesNA19007
Known GenesCTAGE15, CTAGE6, FAM115C, LOC154761
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2940833
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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