A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3922



Internal ID15548580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:100850811..100868534hg38UCSC Ensembl
Outerchr3:100569655..100587378hg19UCSC Ensembl
Outerchr3:102052345..102070068hg18UCSC Ensembl
Outerchr3:102052345..102070068hg17UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg3817724
hg1917724
hg1817724
hg1717724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7839
SamplesNA12156
Known GenesABI3BP
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)nsv3922
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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