A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2894933



Internal ID15599350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177576702..177665790hg38UCSC Ensembl
Innerchr3:177294490..177383578hg19UCSC Ensembl
Innerchr3:178777184..178866272hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3889089
hg1989089
hg1889089
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514189
Supporting Variants
SamplesNA10835
Known GenesLINC00578
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2894933
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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