A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4100



Internal ID15548776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:164582965..164611235hg38UCSC Ensembl
Outerchr3:164300753..164329023hg19UCSC Ensembl
Outerchr3:165783447..165811717hg18UCSC Ensembl
Outerchr3:165783455..165811725hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3828271
hg1928271
hg1828271
hg1728271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4694
SamplesNA19129
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)nsv4100
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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