A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7848



Internal ID15536016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:113040707..113081389hg38UCSC Ensembl
Outerchr3:112759554..112800236hg19UCSC Ensembl
Outerchr3:114242244..114282926hg18UCSC Ensembl
Outerchr3:114242244..114282926hg17UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3840683
hg1940683
hg1840683
hg1740683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951
Supporting Variants
SamplesNA12156
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)nssv7848
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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