A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4064



Internal ID15548736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:151580399..151653198hg38UCSC Ensembl
Outerchr3:151298187..151370986hg19UCSC Ensembl
Outerchr3:152780877..152853676hg18UCSC Ensembl
Outerchr3:152780885..152853684hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3872800
hg1972800
hg1872800
hg1772800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7884, nssv7883
SamplesNA12156
Known GenesMIR548H2
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)nsv4064
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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