A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2949009



Internal ID15745679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55218513..55222617hg38UCSC Ensembl
Innerchr7:55286206..55290310hg19UCSC Ensembl
Innerchr7:55253700..55257804hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg384105
hg194105
hg184105
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514424
Supporting Variants
SamplesNA19150
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2949009
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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