A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2386



Internal ID15540750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:6291239..6336114hg38UCSC Ensembl
Outerchr3:6332926..6377801hg19UCSC Ensembl
Outerchr3:6307926..6352801hg18UCSC Ensembl
Outerchr3:6307926..6352801hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3844876
hg1944876
hg1844876
hg1744876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3684
Supporting Variants
SamplesNA18555
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)nssv2386
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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