A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3726



Internal ID15548364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:20705318..20717354hg38UCSC Ensembl
Outerchr3:20746810..20758846hg19UCSC Ensembl
Outerchr3:20721814..20733850hg18UCSC Ensembl
Outerchr3:20721814..20733850hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385878
hg195878
hg185878
hg175878
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4600, nssv1661
SamplesNA12878, NA19240
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)nsv3726
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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