A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3741



Internal ID15548381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:26382348..26411271hg38UCSC Ensembl
Outerchr3:26423839..26452762hg19UCSC Ensembl
Outerchr3:26398843..26427766hg18UCSC Ensembl
Outerchr3:26398843..26427766hg17UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3828924
hg1928924
hg1828924
hg1728924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6998, nssv1664
SamplesNA12156, 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)nsv3741
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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