A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4062



Internal ID15548734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:150899658..150917379hg38UCSC Ensembl
Outerchr3:150617445..150635166hg19UCSC Ensembl
Outerchr3:152100135..152117856hg18UCSC Ensembl
Outerchr3:152100143..152117864hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3817722
hg1917722
hg1817722
hg1717722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7881
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)nsv4062
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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