A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4055



Internal ID15202040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:149189933..149234745hg38UCSC Ensembl
Outerchr3:148907720..148952532hg19UCSC Ensembl
Outerchr3:150390410..150435222hg18UCSC Ensembl
Outerchr3:150390418..150435230hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3844813
hg1944813
hg1844813
hg1744813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7879
SamplesNA12156
Known GenesCP
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)nsv4055
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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