A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3715



Internal ID15548352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:17472833..17536686hg38UCSC Ensembl
Outerchr3:17514325..17578178hg19UCSC Ensembl
Outerchr3:17489329..17553182hg18UCSC Ensembl
Outerchr3:17489329..17553182hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3863854
hg1963854
hg1863854
hg1763854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5946, nssv1659
SamplesNA19240, NA19129
Known GenesTBC1D5
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)nsv3715
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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