A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2939055



Internal ID15639944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110790684..110792436hg38UCSC Ensembl
Innerchr7:110430740..110432492hg19UCSC Ensembl
Innerchr7:110217976..110219728hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg381753
hg191753
hg181753
Variant TypeCNV gain
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514439
Supporting Variants
SamplesNA12716
Known GenesIMMP2L
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2939055
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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