A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4070



Internal ID15548743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:152586466..152631274hg38UCSC Ensembl
Outerchr3:152304255..152349063hg19UCSC Ensembl
Outerchr3:153786945..153831753hg18UCSC Ensembl
Outerchr3:153786953..153831761hg17UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3844809
hg1944809
hg1844809
hg1744809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7885
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)nsv4070
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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