A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7056



Internal ID15536808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:193153739..193170987hg38UCSC Ensembl
Outerchr3:192871528..192888776hg19UCSC Ensembl
Outerchr3:194354222..194371470hg18UCSC Ensembl
Outerchr3:194354230..194371478hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3817249
hg1917249
hg1817249
hg1717249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4174
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)nssv7056
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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