A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7015



Internal ID15536849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:89612009..89635926hg38UCSC Ensembl
Outerchr3:89661159..89685076hg19UCSC Ensembl
Outerchr3:89743849..89767766hg18UCSC Ensembl
Outerchr3:89743849..89767766hg17UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3823918
hg1923918
hg1823918
hg1723918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3909
Supporting Variants
SamplesNA12156
Known Genes
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)nssv7015
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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