A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4124



Internal ID15202116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:174461292..174478318hg38UCSC Ensembl
Outerchr3:174179082..174196108hg19UCSC Ensembl
Outerchr3:175661776..175678802hg18UCSC Ensembl
Outerchr3:175661784..175678810hg17UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3817027
hg1917027
hg1817027
hg1717027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7896
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)nsv4124
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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