A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3865



Internal ID15548517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:70277757..70322958hg38UCSC Ensembl
Outerchr3:70326908..70372109hg19UCSC Ensembl
Outerchr3:70409598..70454799hg18UCSC Ensembl
Outerchr3:70409598..70454799hg17UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3845202
hg1945202
hg1845202
hg1745202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7822
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)nsv3865
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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