A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv359



Internal ID15544767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:193144139..193177091hg38UCSC Ensembl
Outerchr3:192861928..192894880hg19UCSC Ensembl
Outerchr3:194344622..194377574hg18UCSC Ensembl
Outerchr3:194344630..194377582hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3832953
hg1932953
hg1832953
hg1732953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4174
Supporting Variants
SamplesNA19240
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)nssv359
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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