A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3767



Internal ID15548409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:37908338..37952367hg38UCSC Ensembl
Outerchr3:37949829..37993858hg19UCSC Ensembl
Outerchr3:37924833..37968862hg18UCSC Ensembl
Outerchr3:37924833..37968862hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3844030
hg1944030
hg1844030
hg1744030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7789
SamplesNA12156
Known GenesCTDSPL
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)nsv3767
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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