A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3796



Internal ID15201755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:45809469..45844553hg38UCSC Ensembl
Outerchr3:45850961..45886045hg19UCSC Ensembl
Outerchr3:45825965..45861049hg18UCSC Ensembl
Outerchr3:45825965..45861049hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3835085
hg1935085
hg1835085
hg1735085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7005
SamplesNA12156
Known GenesLZTFL1
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)nsv3796
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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