A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4074



Internal ID15548747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:155301695..155329008hg38UCSC Ensembl
Outerchr3:155019484..155046797hg19UCSC Ensembl
Outerchr3:156502178..156529491hg18UCSC Ensembl
Outerchr3:156502186..156529499hg17UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg386312
hg196312
hg186312
hg176312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv344
SamplesNA19240
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)nsv4074
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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