A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3219



Internal ID15191261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:186851546..186896255hg38UCSC Ensembl
Outerchr3:186569335..186614044hg19UCSC Ensembl
Outerchr3:188052029..188096738hg18UCSC Ensembl
Outerchr3:188052037..188096746hg17UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3844710
hg1944710
hg1844710
hg1744710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4155
Supporting Variants
SamplesNA12878
Known GenesADIPOQ, ADIPOQ-AS1
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv3219
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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